U.S. flag

An official website of the United States government

NM_007294.4(BRCA1):c.5074G>A (p.Asp1692Asn) AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:
Pathogenic/Likely pathogenic (8 submissions)
Last evaluated:
Nov 4, 2022
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000031213.26

Allele description [Variation Report for NM_007294.4(BRCA1):c.5074G>A (p.Asp1692Asn)]

NM_007294.4(BRCA1):c.5074G>A (p.Asp1692Asn)

Gene:
BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q21.31
Genomic location:
Preferred name:
NM_007294.4(BRCA1):c.5074G>A (p.Asp1692Asn)
HGVS:
  • NC_000017.11:g.43067608C>T
  • NG_005905.2:g.150376G>A
  • NM_001407571.1:c.4861G>A
  • NM_001407581.1:c.5140G>A
  • NM_001407582.1:c.5140G>A
  • NM_001407583.1:c.5137G>A
  • NM_001407585.1:c.5137G>A
  • NM_001407587.1:c.5137G>A
  • NM_001407590.1:c.5134G>A
  • NM_001407591.1:c.5134G>A
  • NM_001407593.1:c.5074G>A
  • NM_001407594.1:c.5074G>A
  • NM_001407596.1:c.5074G>A
  • NM_001407597.1:c.5074G>A
  • NM_001407598.1:c.5074G>A
  • NM_001407602.1:c.5074G>A
  • NM_001407603.1:c.5074G>A
  • NM_001407605.1:c.5074G>A
  • NM_001407610.1:c.5071G>A
  • NM_001407611.1:c.5071G>A
  • NM_001407612.1:c.5071G>A
  • NM_001407613.1:c.5071G>A
  • NM_001407614.1:c.5071G>A
  • NM_001407615.1:c.5071G>A
  • NM_001407616.1:c.5071G>A
  • NM_001407617.1:c.5071G>A
  • NM_001407618.1:c.5071G>A
  • NM_001407619.1:c.5071G>A
  • NM_001407620.1:c.5071G>A
  • NM_001407621.1:c.5071G>A
  • NM_001407622.1:c.5071G>A
  • NM_001407623.1:c.5071G>A
  • NM_001407624.1:c.5071G>A
  • NM_001407625.1:c.5071G>A
  • NM_001407626.1:c.5071G>A
  • NM_001407627.1:c.5068G>A
  • NM_001407628.1:c.5068G>A
  • NM_001407629.1:c.5068G>A
  • NM_001407630.1:c.5068G>A
  • NM_001407631.1:c.5068G>A
  • NM_001407632.1:c.5068G>A
  • NM_001407633.1:c.5068G>A
  • NM_001407634.1:c.5068G>A
  • NM_001407635.1:c.5068G>A
  • NM_001407636.1:c.5068G>A
  • NM_001407637.1:c.5068G>A
  • NM_001407638.1:c.5068G>A
  • NM_001407639.1:c.5068G>A
  • NM_001407640.1:c.5068G>A
  • NM_001407641.1:c.5068G>A
  • NM_001407642.1:c.5068G>A
  • NM_001407644.1:c.5065G>A
  • NM_001407645.1:c.5065G>A
  • NM_001407646.1:c.5062G>A
  • NM_001407647.1:c.5059G>A
  • NM_001407648.1:c.5017G>A
  • NM_001407649.1:c.5014G>A
  • NM_001407652.1:c.5074G>A
  • NM_001407653.1:c.4996G>A
  • NM_001407654.1:c.4996G>A
  • NM_001407655.1:c.4996G>A
  • NM_001407656.1:c.4993G>A
  • NM_001407657.1:c.4993G>A
  • NM_001407658.1:c.4993G>A
  • NM_001407659.1:c.4990G>A
  • NM_001407660.1:c.4990G>A
  • NM_001407661.1:c.4990G>A
  • NM_001407662.1:c.4990G>A
  • NM_001407663.1:c.4990G>A
  • NM_001407664.1:c.4951G>A
  • NM_001407665.1:c.4951G>A
  • NM_001407666.1:c.4951G>A
  • NM_001407667.1:c.4951G>A
  • NM_001407668.1:c.4951G>A
  • NM_001407669.1:c.4951G>A
  • NM_001407670.1:c.4948G>A
  • NM_001407671.1:c.4948G>A
  • NM_001407672.1:c.4948G>A
  • NM_001407673.1:c.4948G>A
  • NM_001407674.1:c.4948G>A
  • NM_001407675.1:c.4948G>A
  • NM_001407676.1:c.4948G>A
  • NM_001407677.1:c.4948G>A
  • NM_001407678.1:c.4948G>A
  • NM_001407679.1:c.4948G>A
  • NM_001407680.1:c.4948G>A
  • NM_001407681.1:c.4945G>A
  • NM_001407682.1:c.4945G>A
  • NM_001407683.1:c.4945G>A
  • NM_001407684.1:c.5074G>A
  • NM_001407685.1:c.4945G>A
  • NM_001407686.1:c.4945G>A
  • NM_001407687.1:c.4945G>A
  • NM_001407688.1:c.4945G>A
  • NM_001407689.1:c.4945G>A
  • NM_001407690.1:c.4942G>A
  • NM_001407691.1:c.4942G>A
  • NM_001407692.1:c.4933G>A
  • NM_001407694.1:c.4933G>A
  • NM_001407695.1:c.4933G>A
  • NM_001407696.1:c.4933G>A
  • NM_001407697.1:c.4933G>A
  • NM_001407698.1:c.4933G>A
  • NM_001407724.1:c.4933G>A
  • NM_001407725.1:c.4933G>A
  • NM_001407726.1:c.4933G>A
  • NM_001407727.1:c.4933G>A
  • NM_001407728.1:c.4933G>A
  • NM_001407729.1:c.4933G>A
  • NM_001407730.1:c.4933G>A
  • NM_001407731.1:c.4933G>A
  • NM_001407732.1:c.4930G>A
  • NM_001407733.1:c.4930G>A
  • NM_001407734.1:c.4930G>A
  • NM_001407735.1:c.4930G>A
  • NM_001407736.1:c.4930G>A
  • NM_001407737.1:c.4930G>A
  • NM_001407738.1:c.4930G>A
  • NM_001407739.1:c.4930G>A
  • NM_001407740.1:c.4930G>A
  • NM_001407741.1:c.4930G>A
  • NM_001407742.1:c.4930G>A
  • NM_001407743.1:c.4930G>A
  • NM_001407744.1:c.4930G>A
  • NM_001407745.1:c.4930G>A
  • NM_001407746.1:c.4930G>A
  • NM_001407747.1:c.4930G>A
  • NM_001407748.1:c.4930G>A
  • NM_001407749.1:c.4930G>A
  • NM_001407750.1:c.4930G>A
  • NM_001407751.1:c.4930G>A
  • NM_001407752.1:c.4930G>A
  • NM_001407838.1:c.4927G>A
  • NM_001407839.1:c.4927G>A
  • NM_001407841.1:c.4927G>A
  • NM_001407842.1:c.4927G>A
  • NM_001407843.1:c.4927G>A
  • NM_001407844.1:c.4927G>A
  • NM_001407845.1:c.4927G>A
  • NM_001407846.1:c.4927G>A
  • NM_001407847.1:c.4927G>A
  • NM_001407848.1:c.4927G>A
  • NM_001407849.1:c.4927G>A
  • NM_001407850.1:c.4927G>A
  • NM_001407851.1:c.4927G>A
  • NM_001407852.1:c.4927G>A
  • NM_001407853.1:c.4927G>A
  • NM_001407854.1:c.5074G>A
  • NM_001407858.1:c.5071G>A
  • NM_001407859.1:c.5071G>A
  • NM_001407860.1:c.5071G>A
  • NM_001407861.1:c.5068G>A
  • NM_001407862.1:c.4873G>A
  • NM_001407863.1:c.4948G>A
  • NM_001407874.1:c.4867G>A
  • NM_001407875.1:c.4867G>A
  • NM_001407879.1:c.4864G>A
  • NM_001407881.1:c.4864G>A
  • NM_001407882.1:c.4864G>A
  • NM_001407884.1:c.4864G>A
  • NM_001407885.1:c.4864G>A
  • NM_001407886.1:c.4864G>A
  • NM_001407887.1:c.4864G>A
  • NM_001407889.1:c.4864G>A
  • NM_001407894.1:c.4861G>A
  • NM_001407895.1:c.4861G>A
  • NM_001407896.1:c.4861G>A
  • NM_001407897.1:c.4861G>A
  • NM_001407898.1:c.4861G>A
  • NM_001407899.1:c.4861G>A
  • NM_001407900.1:c.4861G>A
  • NM_001407902.1:c.4861G>A
  • NM_001407904.1:c.4861G>A
  • NM_001407906.1:c.4861G>A
  • NM_001407907.1:c.4861G>A
  • NM_001407908.1:c.4861G>A
  • NM_001407909.1:c.4861G>A
  • NM_001407910.1:c.4861G>A
  • NM_001407915.1:c.4858G>A
  • NM_001407916.1:c.4858G>A
  • NM_001407917.1:c.4858G>A
  • NM_001407918.1:c.4858G>A
  • NM_001407919.1:c.4951G>A
  • NM_001407920.1:c.4810G>A
  • NM_001407921.1:c.4810G>A
  • NM_001407922.1:c.4810G>A
  • NM_001407923.1:c.4810G>A
  • NM_001407924.1:c.4810G>A
  • NM_001407925.1:c.4810G>A
  • NM_001407926.1:c.4810G>A
  • NM_001407927.1:c.4807G>A
  • NM_001407928.1:c.4807G>A
  • NM_001407929.1:c.4807G>A
  • NM_001407930.1:c.4807G>A
  • NM_001407931.1:c.4807G>A
  • NM_001407932.1:c.4807G>A
  • NM_001407933.1:c.4807G>A
  • NM_001407934.1:c.4804G>A
  • NM_001407935.1:c.4804G>A
  • NM_001407936.1:c.4804G>A
  • NM_001407937.1:c.4951G>A
  • NM_001407938.1:c.4951G>A
  • NM_001407939.1:c.4948G>A
  • NM_001407940.1:c.4948G>A
  • NM_001407941.1:c.4945G>A
  • NM_001407942.1:c.4933G>A
  • NM_001407943.1:c.4930G>A
  • NM_001407944.1:c.4930G>A
  • NM_001407945.1:c.4930G>A
  • NM_001407946.1:c.4741G>A
  • NM_001407947.1:c.4741G>A
  • NM_001407948.1:c.4741G>A
  • NM_001407949.1:c.4741G>A
  • NM_001407950.1:c.4738G>A
  • NM_001407951.1:c.4738G>A
  • NM_001407952.1:c.4738G>A
  • NM_001407953.1:c.4738G>A
  • NM_001407954.1:c.4738G>A
  • NM_001407955.1:c.4738G>A
  • NM_001407956.1:c.4735G>A
  • NM_001407957.1:c.4735G>A
  • NM_001407958.1:c.4735G>A
  • NM_001407959.1:c.4693G>A
  • NM_001407960.1:c.4690G>A
  • NM_001407962.1:c.4690G>A
  • NM_001407963.1:c.4687G>A
  • NM_001407964.1:c.4612G>A
  • NM_001407965.1:c.4567G>A
  • NM_001407966.1:c.4186G>A
  • NM_001407967.1:c.4183G>A
  • NM_001407968.1:c.2470G>A
  • NM_001407969.1:c.2467G>A
  • NM_001407970.1:c.1831G>A
  • NM_001407971.1:c.1831G>A
  • NM_001407972.1:c.1828G>A
  • NM_001407973.1:c.1765G>A
  • NM_001407974.1:c.1765G>A
  • NM_001407975.1:c.1765G>A
  • NM_001407976.1:c.1765G>A
  • NM_001407977.1:c.1765G>A
  • NM_001407978.1:c.1765G>A
  • NM_001407979.1:c.1762G>A
  • NM_001407980.1:c.1762G>A
  • NM_001407981.1:c.1762G>A
  • NM_001407982.1:c.1762G>A
  • NM_001407983.1:c.1762G>A
  • NM_001407984.1:c.1762G>A
  • NM_001407985.1:c.1762G>A
  • NM_001407986.1:c.1762G>A
  • NM_001407990.1:c.1762G>A
  • NM_001407991.1:c.1762G>A
  • NM_001407992.1:c.1762G>A
  • NM_001407993.1:c.1762G>A
  • NM_001408392.1:c.1759G>A
  • NM_001408396.1:c.1759G>A
  • NM_001408397.1:c.1759G>A
  • NM_001408398.1:c.1759G>A
  • NM_001408399.1:c.1759G>A
  • NM_001408400.1:c.1759G>A
  • NM_001408401.1:c.1759G>A
  • NM_001408402.1:c.1759G>A
  • NM_001408403.1:c.1759G>A
  • NM_001408404.1:c.1759G>A
  • NM_001408406.1:c.1756G>A
  • NM_001408407.1:c.1756G>A
  • NM_001408408.1:c.1756G>A
  • NM_001408409.1:c.1753G>A
  • NM_001408410.1:c.1690G>A
  • NM_001408411.1:c.1687G>A
  • NM_001408412.1:c.1684G>A
  • NM_001408413.1:c.1684G>A
  • NM_001408414.1:c.1684G>A
  • NM_001408415.1:c.1684G>A
  • NM_001408416.1:c.1684G>A
  • NM_001408418.1:c.1648G>A
  • NM_001408419.1:c.1648G>A
  • NM_001408420.1:c.1648G>A
  • NM_001408421.1:c.1645G>A
  • NM_001408422.1:c.1645G>A
  • NM_001408423.1:c.1645G>A
  • NM_001408424.1:c.1645G>A
  • NM_001408425.1:c.1642G>A
  • NM_001408426.1:c.1642G>A
  • NM_001408427.1:c.1642G>A
  • NM_001408428.1:c.1642G>A
  • NM_001408429.1:c.1642G>A
  • NM_001408430.1:c.1642G>A
  • NM_001408431.1:c.1642G>A
  • NM_001408432.1:c.1639G>A
  • NM_001408433.1:c.1639G>A
  • NM_001408434.1:c.1639G>A
  • NM_001408435.1:c.1639G>A
  • NM_001408436.1:c.1639G>A
  • NM_001408437.1:c.1639G>A
  • NM_001408438.1:c.1639G>A
  • NM_001408439.1:c.1639G>A
  • NM_001408440.1:c.1639G>A
  • NM_001408441.1:c.1639G>A
  • NM_001408442.1:c.1639G>A
  • NM_001408443.1:c.1639G>A
  • NM_001408444.1:c.1639G>A
  • NM_001408445.1:c.1636G>A
  • NM_001408446.1:c.1636G>A
  • NM_001408447.1:c.1636G>A
  • NM_001408448.1:c.1636G>A
  • NM_001408450.1:c.1636G>A
  • NM_001408451.1:c.1630G>A
  • NM_001408452.1:c.1624G>A
  • NM_001408453.1:c.1624G>A
  • NM_001408454.1:c.1624G>A
  • NM_001408455.1:c.1624G>A
  • NM_001408456.1:c.1624G>A
  • NM_001408457.1:c.1624G>A
  • NM_001408458.1:c.1621G>A
  • NM_001408459.1:c.1621G>A
  • NM_001408460.1:c.1621G>A
  • NM_001408461.1:c.1621G>A
  • NM_001408462.1:c.1621G>A
  • NM_001408463.1:c.1621G>A
  • NM_001408464.1:c.1621G>A
  • NM_001408465.1:c.1621G>A
  • NM_001408466.1:c.1621G>A
  • NM_001408467.1:c.1621G>A
  • NM_001408468.1:c.1618G>A
  • NM_001408469.1:c.1618G>A
  • NM_001408470.1:c.1618G>A
  • NM_001408472.1:c.1762G>A
  • NM_001408473.1:c.1759G>A
  • NM_001408474.1:c.1564G>A
  • NM_001408475.1:c.1561G>A
  • NM_001408476.1:c.1561G>A
  • NM_001408478.1:c.1555G>A
  • NM_001408479.1:c.1555G>A
  • NM_001408480.1:c.1555G>A
  • NM_001408481.1:c.1552G>A
  • NM_001408482.1:c.1552G>A
  • NM_001408483.1:c.1552G>A
  • NM_001408484.1:c.1552G>A
  • NM_001408485.1:c.1552G>A
  • NM_001408489.1:c.1552G>A
  • NM_001408490.1:c.1552G>A
  • NM_001408491.1:c.1552G>A
  • NM_001408492.1:c.1549G>A
  • NM_001408493.1:c.1549G>A
  • NM_001408494.1:c.1525G>A
  • NM_001408495.1:c.1519G>A
  • NM_001408496.1:c.1501G>A
  • NM_001408497.1:c.1501G>A
  • NM_001408498.1:c.1501G>A
  • NM_001408499.1:c.1501G>A
  • NM_001408500.1:c.1501G>A
  • NM_001408501.1:c.1501G>A
  • NM_001408502.1:c.1498G>A
  • NM_001408503.1:c.1498G>A
  • NM_001408504.1:c.1498G>A
  • NM_001408505.1:c.1495G>A
  • NM_001408506.1:c.1438G>A
  • NM_001408507.1:c.1435G>A
  • NM_001408508.1:c.1426G>A
  • NM_001408509.1:c.1423G>A
  • NM_001408510.1:c.1384G>A
  • NM_001408511.1:c.1381G>A
  • NM_001408512.1:c.1261G>A
  • NM_001408513.1:c.1234G>A
  • NM_007294.4:c.5074G>AMANE SELECT
  • NM_007297.4:c.4933G>A
  • NM_007298.4:c.1762G>A
  • NM_007299.4:c.1762G>A
  • NM_007300.4:c.5137G>A
  • NM_007304.2:c.1762G>A
  • NP_001394500.1:p.Asp1621Asn
  • NP_001394510.1:p.Asp1714Asn
  • NP_001394511.1:p.Asp1714Asn
  • NP_001394512.1:p.Asp1713Asn
  • NP_001394514.1:p.Asp1713Asn
  • NP_001394516.1:p.Asp1713Asn
  • NP_001394519.1:p.Asp1712Asn
  • NP_001394520.1:p.Asp1712Asn
  • NP_001394522.1:p.Asp1692Asn
  • NP_001394523.1:p.Asp1692Asn
  • NP_001394525.1:p.Asp1692Asn
  • NP_001394526.1:p.Asp1692Asn
  • NP_001394527.1:p.Asp1692Asn
  • NP_001394531.1:p.Asp1692Asn
  • NP_001394532.1:p.Asp1692Asn
  • NP_001394534.1:p.Asp1692Asn
  • NP_001394539.1:p.Asp1691Asn
  • NP_001394540.1:p.Asp1691Asn
  • NP_001394541.1:p.Asp1691Asn
  • NP_001394542.1:p.Asp1691Asn
  • NP_001394543.1:p.Asp1691Asn
  • NP_001394544.1:p.Asp1691Asn
  • NP_001394545.1:p.Asp1691Asn
  • NP_001394546.1:p.Asp1691Asn
  • NP_001394547.1:p.Asp1691Asn
  • NP_001394548.1:p.Asp1691Asn
  • NP_001394549.1:p.Asp1691Asn
  • NP_001394550.1:p.Asp1691Asn
  • NP_001394551.1:p.Asp1691Asn
  • NP_001394552.1:p.Asp1691Asn
  • NP_001394553.1:p.Asp1691Asn
  • NP_001394554.1:p.Asp1691Asn
  • NP_001394555.1:p.Asp1691Asn
  • NP_001394556.1:p.Asp1690Asn
  • NP_001394557.1:p.Asp1690Asn
  • NP_001394558.1:p.Asp1690Asn
  • NP_001394559.1:p.Asp1690Asn
  • NP_001394560.1:p.Asp1690Asn
  • NP_001394561.1:p.Asp1690Asn
  • NP_001394562.1:p.Asp1690Asn
  • NP_001394563.1:p.Asp1690Asn
  • NP_001394564.1:p.Asp1690Asn
  • NP_001394565.1:p.Asp1690Asn
  • NP_001394566.1:p.Asp1690Asn
  • NP_001394567.1:p.Asp1690Asn
  • NP_001394568.1:p.Asp1690Asn
  • NP_001394569.1:p.Asp1690Asn
  • NP_001394570.1:p.Asp1690Asn
  • NP_001394571.1:p.Asp1690Asn
  • NP_001394573.1:p.Asp1689Asn
  • NP_001394574.1:p.Asp1689Asn
  • NP_001394575.1:p.Asp1688Asn
  • NP_001394576.1:p.Asp1687Asn
  • NP_001394577.1:p.Asp1673Asn
  • NP_001394578.1:p.Asp1672Asn
  • NP_001394581.1:p.Gly1692Arg
  • NP_001394582.1:p.Asp1666Asn
  • NP_001394583.1:p.Asp1666Asn
  • NP_001394584.1:p.Asp1666Asn
  • NP_001394585.1:p.Asp1665Asn
  • NP_001394586.1:p.Asp1665Asn
  • NP_001394587.1:p.Asp1665Asn
  • NP_001394588.1:p.Asp1664Asn
  • NP_001394589.1:p.Asp1664Asn
  • NP_001394590.1:p.Asp1664Asn
  • NP_001394591.1:p.Asp1664Asn
  • NP_001394592.1:p.Asp1664Asn
  • NP_001394593.1:p.Asp1651Asn
  • NP_001394594.1:p.Asp1651Asn
  • NP_001394595.1:p.Asp1651Asn
  • NP_001394596.1:p.Asp1651Asn
  • NP_001394597.1:p.Asp1651Asn
  • NP_001394598.1:p.Asp1651Asn
  • NP_001394599.1:p.Asp1650Asn
  • NP_001394600.1:p.Asp1650Asn
  • NP_001394601.1:p.Asp1650Asn
  • NP_001394602.1:p.Asp1650Asn
  • NP_001394603.1:p.Asp1650Asn
  • NP_001394604.1:p.Asp1650Asn
  • NP_001394605.1:p.Asp1650Asn
  • NP_001394606.1:p.Asp1650Asn
  • NP_001394607.1:p.Asp1650Asn
  • NP_001394608.1:p.Asp1650Asn
  • NP_001394609.1:p.Asp1650Asn
  • NP_001394610.1:p.Asp1649Asn
  • NP_001394611.1:p.Asp1649Asn
  • NP_001394612.1:p.Asp1649Asn
  • NP_001394613.1:p.Asp1692Asn
  • NP_001394614.1:p.Asp1649Asn
  • NP_001394615.1:p.Asp1649Asn
  • NP_001394616.1:p.Asp1649Asn
  • NP_001394617.1:p.Asp1649Asn
  • NP_001394618.1:p.Asp1649Asn
  • NP_001394619.1:p.Asp1648Asn
  • NP_001394620.1:p.Asp1648Asn
  • NP_001394621.1:p.Asp1645Asn
  • NP_001394623.1:p.Asp1645Asn
  • NP_001394624.1:p.Asp1645Asn
  • NP_001394625.1:p.Asp1645Asn
  • NP_001394626.1:p.Asp1645Asn
  • NP_001394627.1:p.Asp1645Asn
  • NP_001394653.1:p.Asp1645Asn
  • NP_001394654.1:p.Asp1645Asn
  • NP_001394655.1:p.Asp1645Asn
  • NP_001394656.1:p.Asp1645Asn
  • NP_001394657.1:p.Asp1645Asn
  • NP_001394658.1:p.Asp1645Asn
  • NP_001394659.1:p.Asp1645Asn
  • NP_001394660.1:p.Asp1645Asn
  • NP_001394661.1:p.Asp1644Asn
  • NP_001394662.1:p.Asp1644Asn
  • NP_001394663.1:p.Asp1644Asn
  • NP_001394664.1:p.Asp1644Asn
  • NP_001394665.1:p.Asp1644Asn
  • NP_001394666.1:p.Asp1644Asn
  • NP_001394667.1:p.Asp1644Asn
  • NP_001394668.1:p.Asp1644Asn
  • NP_001394669.1:p.Asp1644Asn
  • NP_001394670.1:p.Asp1644Asn
  • NP_001394671.1:p.Asp1644Asn
  • NP_001394672.1:p.Asp1644Asn
  • NP_001394673.1:p.Asp1644Asn
  • NP_001394674.1:p.Asp1644Asn
  • NP_001394675.1:p.Asp1644Asn
  • NP_001394676.1:p.Asp1644Asn
  • NP_001394677.1:p.Asp1644Asn
  • NP_001394678.1:p.Asp1644Asn
  • NP_001394679.1:p.Asp1644Asn
  • NP_001394680.1:p.Asp1644Asn
  • NP_001394681.1:p.Asp1644Asn
  • NP_001394767.1:p.Asp1643Asn
  • NP_001394768.1:p.Asp1643Asn
  • NP_001394770.1:p.Asp1643Asn
  • NP_001394771.1:p.Asp1643Asn
  • NP_001394772.1:p.Asp1643Asn
  • NP_001394773.1:p.Asp1643Asn
  • NP_001394774.1:p.Asp1643Asn
  • NP_001394775.1:p.Asp1643Asn
  • NP_001394776.1:p.Asp1643Asn
  • NP_001394777.1:p.Asp1643Asn
  • NP_001394778.1:p.Asp1643Asn
  • NP_001394779.1:p.Asp1643Asn
  • NP_001394780.1:p.Asp1643Asn
  • NP_001394781.1:p.Asp1643Asn
  • NP_001394782.1:p.Asp1643Asn
  • NP_001394783.1:p.Asp1692Asn
  • NP_001394787.1:p.Asp1691Asn
  • NP_001394788.1:p.Asp1691Asn
  • NP_001394789.1:p.Asp1691Asn
  • NP_001394790.1:p.Asp1690Asn
  • NP_001394791.1:p.Asp1625Asn
  • NP_001394792.1:p.Gly1650Arg
  • NP_001394803.1:p.Asp1623Asn
  • NP_001394804.1:p.Asp1623Asn
  • NP_001394808.1:p.Asp1622Asn
  • NP_001394810.1:p.Asp1622Asn
  • NP_001394811.1:p.Asp1622Asn
  • NP_001394813.1:p.Asp1622Asn
  • NP_001394814.1:p.Asp1622Asn
  • NP_001394815.1:p.Asp1622Asn
  • NP_001394816.1:p.Asp1622Asn
  • NP_001394818.1:p.Asp1622Asn
  • NP_001394823.1:p.Asp1621Asn
  • NP_001394824.1:p.Asp1621Asn
  • NP_001394825.1:p.Asp1621Asn
  • NP_001394826.1:p.Asp1621Asn
  • NP_001394827.1:p.Asp1621Asn
  • NP_001394828.1:p.Asp1621Asn
  • NP_001394829.1:p.Asp1621Asn
  • NP_001394831.1:p.Asp1621Asn
  • NP_001394833.1:p.Asp1621Asn
  • NP_001394835.1:p.Asp1621Asn
  • NP_001394836.1:p.Asp1621Asn
  • NP_001394837.1:p.Asp1621Asn
  • NP_001394838.1:p.Asp1621Asn
  • NP_001394839.1:p.Asp1621Asn
  • NP_001394844.1:p.Asp1620Asn
  • NP_001394845.1:p.Asp1620Asn
  • NP_001394846.1:p.Asp1620Asn
  • NP_001394847.1:p.Asp1620Asn
  • NP_001394848.1:p.Asp1651Asn
  • NP_001394849.1:p.Asp1604Asn
  • NP_001394850.1:p.Asp1604Asn
  • NP_001394851.1:p.Asp1604Asn
  • NP_001394852.1:p.Asp1604Asn
  • NP_001394853.1:p.Asp1604Asn
  • NP_001394854.1:p.Asp1604Asn
  • NP_001394855.1:p.Asp1604Asn
  • NP_001394856.1:p.Asp1603Asn
  • NP_001394857.1:p.Asp1603Asn
  • NP_001394858.1:p.Asp1603Asn
  • NP_001394859.1:p.Asp1603Asn
  • NP_001394860.1:p.Asp1603Asn
  • NP_001394861.1:p.Asp1603Asn
  • NP_001394862.1:p.Asp1603Asn
  • NP_001394863.1:p.Asp1602Asn
  • NP_001394864.1:p.Asp1602Asn
  • NP_001394865.1:p.Asp1602Asn
  • NP_001394866.1:p.Asp1651Asn
  • NP_001394867.1:p.Asp1651Asn
  • NP_001394868.1:p.Asp1650Asn
  • NP_001394869.1:p.Asp1650Asn
  • NP_001394870.1:p.Asp1649Asn
  • NP_001394871.1:p.Asp1645Asn
  • NP_001394872.1:p.Asp1644Asn
  • NP_001394873.1:p.Asp1644Asn
  • NP_001394874.1:p.Asp1644Asn
  • NP_001394875.1:p.Asp1581Asn
  • NP_001394876.1:p.Asp1581Asn
  • NP_001394877.1:p.Asp1581Asn
  • NP_001394878.1:p.Asp1581Asn
  • NP_001394879.1:p.Asp1580Asn
  • NP_001394880.1:p.Asp1580Asn
  • NP_001394881.1:p.Asp1580Asn
  • NP_001394882.1:p.Asp1580Asn
  • NP_001394883.1:p.Asp1580Asn
  • NP_001394884.1:p.Asp1580Asn
  • NP_001394885.1:p.Asp1579Asn
  • NP_001394886.1:p.Asp1579Asn
  • NP_001394887.1:p.Asp1579Asn
  • NP_001394888.1:p.Asp1565Asn
  • NP_001394889.1:p.Asp1564Asn
  • NP_001394891.1:p.Asp1564Asn
  • NP_001394892.1:p.Asp1563Asn
  • NP_001394893.1:p.Asp1538Asn
  • NP_001394894.1:p.Asp1523Asn
  • NP_001394895.1:p.Asp1396Asn
  • NP_001394896.1:p.Asp1395Asn
  • NP_001394897.1:p.Asp824Asn
  • NP_001394898.1:p.Asp823Asn
  • NP_001394899.1:p.Asp611Asn
  • NP_001394900.1:p.Asp611Asn
  • NP_001394901.1:p.Asp610Asn
  • NP_001394902.1:p.Asp589Asn
  • NP_001394903.1:p.Asp589Asn
  • NP_001394904.1:p.Asp589Asn
  • NP_001394905.1:p.Asp589Asn
  • NP_001394906.1:p.Asp589Asn
  • NP_001394907.1:p.Asp589Asn
  • NP_001394908.1:p.Asp588Asn
  • NP_001394909.1:p.Asp588Asn
  • NP_001394910.1:p.Asp588Asn
  • NP_001394911.1:p.Asp588Asn
  • NP_001394912.1:p.Asp588Asn
  • NP_001394913.1:p.Asp588Asn
  • NP_001394914.1:p.Asp588Asn
  • NP_001394915.1:p.Asp588Asn
  • NP_001394919.1:p.Asp588Asn
  • NP_001394920.1:p.Asp588Asn
  • NP_001394921.1:p.Asp588Asn
  • NP_001394922.1:p.Asp588Asn
  • NP_001395321.1:p.Asp587Asn
  • NP_001395325.1:p.Asp587Asn
  • NP_001395326.1:p.Asp587Asn
  • NP_001395327.1:p.Asp587Asn
  • NP_001395328.1:p.Asp587Asn
  • NP_001395329.1:p.Asp587Asn
  • NP_001395330.1:p.Asp587Asn
  • NP_001395331.1:p.Asp587Asn
  • NP_001395332.1:p.Asp587Asn
  • NP_001395333.1:p.Asp587Asn
  • NP_001395335.1:p.Asp586Asn
  • NP_001395336.1:p.Asp586Asn
  • NP_001395337.1:p.Asp586Asn
  • NP_001395338.1:p.Asp585Asn
  • NP_001395339.1:p.Asp564Asn
  • NP_001395340.1:p.Asp563Asn
  • NP_001395341.1:p.Asp562Asn
  • NP_001395342.1:p.Asp562Asn
  • NP_001395343.1:p.Asp562Asn
  • NP_001395344.1:p.Asp562Asn
  • NP_001395345.1:p.Asp562Asn
  • NP_001395347.1:p.Asp550Asn
  • NP_001395348.1:p.Asp550Asn
  • NP_001395349.1:p.Asp550Asn
  • NP_001395350.1:p.Asp549Asn
  • NP_001395351.1:p.Asp549Asn
  • NP_001395352.1:p.Asp549Asn
  • NP_001395353.1:p.Asp549Asn
  • NP_001395354.1:p.Asp548Asn
  • NP_001395355.1:p.Asp548Asn
  • NP_001395356.1:p.Asp548Asn
  • NP_001395357.1:p.Asp548Asn
  • NP_001395358.1:p.Asp548Asn
  • NP_001395359.1:p.Asp548Asn
  • NP_001395360.1:p.Asp548Asn
  • NP_001395361.1:p.Asp547Asn
  • NP_001395362.1:p.Asp547Asn
  • NP_001395363.1:p.Asp547Asn
  • NP_001395364.1:p.Asp547Asn
  • NP_001395365.1:p.Asp547Asn
  • NP_001395366.1:p.Asp547Asn
  • NP_001395367.1:p.Asp547Asn
  • NP_001395368.1:p.Asp547Asn
  • NP_001395369.1:p.Asp547Asn
  • NP_001395370.1:p.Asp547Asn
  • NP_001395371.1:p.Asp547Asn
  • NP_001395372.1:p.Asp547Asn
  • NP_001395373.1:p.Asp547Asn
  • NP_001395374.1:p.Asp546Asn
  • NP_001395375.1:p.Asp546Asn
  • NP_001395376.1:p.Asp546Asn
  • NP_001395377.1:p.Asp546Asn
  • NP_001395379.1:p.Asp546Asn
  • NP_001395380.1:p.Asp544Asn
  • NP_001395381.1:p.Asp542Asn
  • NP_001395382.1:p.Asp542Asn
  • NP_001395383.1:p.Asp542Asn
  • NP_001395384.1:p.Asp542Asn
  • NP_001395385.1:p.Asp542Asn
  • NP_001395386.1:p.Asp542Asn
  • NP_001395387.1:p.Asp541Asn
  • NP_001395388.1:p.Asp541Asn
  • NP_001395389.1:p.Asp541Asn
  • NP_001395390.1:p.Asp541Asn
  • NP_001395391.1:p.Asp541Asn
  • NP_001395392.1:p.Asp541Asn
  • NP_001395393.1:p.Asp541Asn
  • NP_001395394.1:p.Asp541Asn
  • NP_001395395.1:p.Asp541Asn
  • NP_001395396.1:p.Asp541Asn
  • NP_001395397.1:p.Asp540Asn
  • NP_001395398.1:p.Asp540Asn
  • NP_001395399.1:p.Asp540Asn
  • NP_001395401.1:p.Asp588Asn
  • NP_001395402.1:p.Asp587Asn
  • NP_001395403.1:p.Asp522Asn
  • NP_001395404.1:p.Asp521Asn
  • NP_001395405.1:p.Asp521Asn
  • NP_001395407.1:p.Asp519Asn
  • NP_001395408.1:p.Asp519Asn
  • NP_001395409.1:p.Asp519Asn
  • NP_001395410.1:p.Asp518Asn
  • NP_001395411.1:p.Asp518Asn
  • NP_001395412.1:p.Asp518Asn
  • NP_001395413.1:p.Asp518Asn
  • NP_001395414.1:p.Asp518Asn
  • NP_001395418.1:p.Asp518Asn
  • NP_001395419.1:p.Asp518Asn
  • NP_001395420.1:p.Asp518Asn
  • NP_001395421.1:p.Asp517Asn
  • NP_001395422.1:p.Asp517Asn
  • NP_001395423.1:p.Asp509Asn
  • NP_001395424.1:p.Asp507Asn
  • NP_001395425.1:p.Asp501Asn
  • NP_001395426.1:p.Asp501Asn
  • NP_001395427.1:p.Asp501Asn
  • NP_001395428.1:p.Asp501Asn
  • NP_001395429.1:p.Asp501Asn
  • NP_001395430.1:p.Asp501Asn
  • NP_001395431.1:p.Asp500Asn
  • NP_001395432.1:p.Asp500Asn
  • NP_001395433.1:p.Asp500Asn
  • NP_001395434.1:p.Asp499Asn
  • NP_001395435.1:p.Asp480Asn
  • NP_001395436.1:p.Asp479Asn
  • NP_001395437.1:p.Asp476Asn
  • NP_001395438.1:p.Asp475Asn
  • NP_001395439.1:p.Asp462Asn
  • NP_001395440.1:p.Asp461Asn
  • NP_001395441.1:p.Asp421Asn
  • NP_001395442.1:p.Asp412Asn
  • NP_009225.1:p.Asp1692Asn
  • NP_009225.1:p.Asp1692Asn
  • NP_009228.2:p.Asp1645Asn
  • NP_009229.2:p.Asp588Asn
  • NP_009229.2:p.Asp588Asn
  • NP_009230.2:p.Asp588Asn
  • NP_009231.2:p.Asp1713Asn
  • NP_009235.2:p.Asp588Asn
  • LRG_292t1:c.5074G>A
  • LRG_292:g.150376G>A
  • LRG_292p1:p.Asp1692Asn
  • NC_000017.10:g.41219625C>T
  • NM_007294.3:c.5074G>A
  • NM_007298.3:c.1762G>A
  • NR_027676.2:n.5251G>A
  • U14680.1:n.5193G>A
Nucleotide change:
5193G>A
Protein change:
D1395N
Links:
dbSNP: rs80187739
NCBI 1000 Genomes Browser:
rs80187739
Molecular consequence:
  • NM_001407571.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.5140G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.5140G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.5137G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.5137G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.5137G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.5134G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.5134G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.5065G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.5065G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.5062G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.5059G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.5017G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.5014G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.4996G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.4996G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.4996G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.4993G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.4993G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.4993G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.4990G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.4990G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.4990G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.4990G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.4990G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.4951G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.4951G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.4951G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.4951G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.4951G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.4951G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.4945G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.4945G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.4945G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.4945G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.4945G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.4945G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.4945G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.4945G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.4942G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.4942G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.4927G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.5071G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.5068G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.4873G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.4867G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.4867G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.4864G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.4864G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.4864G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.4864G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.4864G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.4864G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.4864G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.4864G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.4861G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.4858G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.4858G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.4858G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.4858G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.4951G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.4810G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.4810G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.4810G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.4810G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.4810G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.4810G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.4810G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.4807G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.4807G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.4807G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.4807G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.4807G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.4807G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.4807G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.4804G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.4804G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.4804G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.4951G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.4951G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.4948G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.4945G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.4930G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.4741G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.4741G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.4741G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.4741G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.4738G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.4738G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.4738G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.4738G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.4738G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.4738G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.4735G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.4735G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.4735G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.4693G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.4690G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.4690G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.4687G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.4612G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.4567G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.4186G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.4183G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.2470G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.2467G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.1831G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.1831G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.1828G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407993.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408392.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408396.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408397.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408398.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408399.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408403.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408404.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.1756G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408407.1:c.1756G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.1756G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.1753G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408410.1:c.1690G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.1687G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408412.1:c.1684G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.1684G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408414.1:c.1684G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408415.1:c.1684G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.1684G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.1648G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.1648G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.1648G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.1645G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408422.1:c.1645G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408423.1:c.1645G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.1645G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.1642G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.1642G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.1642G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.1642G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.1642G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.1642G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408431.1:c.1642G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408436.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408437.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408438.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408439.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408440.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.1639G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408445.1:c.1636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408446.1:c.1636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408447.1:c.1636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408448.1:c.1636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408450.1:c.1636G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408451.1:c.1630G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408452.1:c.1624G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408453.1:c.1624G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408454.1:c.1624G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408455.1:c.1624G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408456.1:c.1624G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408457.1:c.1624G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408458.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408459.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408460.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408461.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408462.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408463.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408464.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408465.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408466.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408467.1:c.1621G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408468.1:c.1618G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408469.1:c.1618G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408470.1:c.1618G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408472.1:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408473.1:c.1759G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.1564G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.1561G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408476.1:c.1561G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408478.1:c.1555G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408479.1:c.1555G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408480.1:c.1555G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408481.1:c.1552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408482.1:c.1552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408483.1:c.1552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408484.1:c.1552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408485.1:c.1552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408489.1:c.1552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408490.1:c.1552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408491.1:c.1552G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408492.1:c.1549G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408493.1:c.1549G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.1525G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408495.1:c.1519G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408496.1:c.1501G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408497.1:c.1501G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408498.1:c.1501G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408499.1:c.1501G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408500.1:c.1501G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408501.1:c.1501G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408502.1:c.1498G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408503.1:c.1498G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408504.1:c.1498G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408505.1:c.1495G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408506.1:c.1438G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408507.1:c.1435G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408508.1:c.1426G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408509.1:c.1423G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408510.1:c.1384G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408511.1:c.1381G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408512.1:c.1261G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408513.1:c.1234G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.5074G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.4933G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007298.4:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007299.4:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.5137G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007304.2:c.1762G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_027676.2:n.5251G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Functional consequence:
functionally_abnormal [Sequence Ontology: SO:0002218] - Comment(s)
Observations:
7

Condition(s)

Name:
Breast-ovarian cancer, familial, susceptibility to, 1 (BROVCA1)
Synonyms:
OVARIAN CANCER, SUSCEPTIBILITY TO; Breast cancer, familial 1
Identifiers:
MONDO: MONDO:0011450; MedGen: C2676676; Orphanet: 145; OMIM: 604370

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000053813Sharing Clinical Reports Project (SCRP)
no assertion criteria provided
Likely pathogenic
(Jul 25, 2006)
germlineclinical testing

SCV000145293Breast Cancer Information Core (BIC) (BRCA1)
no assertion criteria provided
Pathogenic
(May 29, 2002)
germlineclinical testing

SCV000326135Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), c/o University of Cambridge
criteria provided, single submitter

(CIMBA Mutation Classification guidelines May 2016)
Pathogenic
(Oct 2, 2015)
germlineclinical testing

CIMBA_Mutation_Classification_guidelines_May16.pdf,

Citation Link,

SCV001244020Brotman Baty Institute, University of Washington
no classification provided
not providednot applicablein vitro

PubMed (1)
[See all records that cite this PMID]

Citation Link,

SCV002578917MGZ Medical Genetics Center
criteria provided, single submitter

(ACMG Guidelines, 2015)
Pathogenic
(May 20, 2022)
germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

SCV003843144St. Jude Molecular Pathology, St. Jude Children's Research Hospital
criteria provided, single submitter

(St. Jude Assertion Criteria 2020)
Likely pathogenic
(Nov 4, 2022)
germlineclinical testing

Citation Link,

SCV004022171deCODE genetics, Amgen
no assertion criteria provided
Pathogenic
(Jul 21, 2023)
germlineresearch

SCV004228368Department of Medical and Surgical Sciences, University of Bologna
no assertion criteria provided
Likely pathogenic
(Sep 1, 2023)
germlineclinical testing

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes7not providednot providednot providednot providedclinical testing
not providedgermlineunknownnot provided7not providednot providednot providedclinical testing
not providedgermlinenot provided1not providednot provided1not providedclinical testing
not providednot applicablenot applicablenot providednot providednot providednot providednot providedin vitro
Africangermlineyes1not providednot providednot providednot providedclinical testing
African Americangermlineyes1not providednot providednot providednot providedclinical testing
Icelandicgermlineyes70not providednot providednot providednot providedresearch
Latin American, Caribbeangermlineyes1not providednot providednot providednot providedclinical testing
Western Europeangermlineyes2not providednot providednot providednot providedclinical testing

Citations

PubMed

Accurate classification of BRCA1 variants with saturation genome editing.

Findlay GM, Daza RM, Martin B, Zhang MD, Leith AP, Gasperini M, Janizek JD, Huang X, Starita LM, Shendure J.

Nature. 2018 Oct;562(7726):217-222. doi: 10.1038/s41586-018-0461-z. Epub 2018 Sep 12.

PubMed [citation]
PMID:
30209399
PMCID:
PMC6181777

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Sharing Clinical Reports Project (SCRP), SCV000053813.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot provided1not providednot providednot providednot providednot provided See 1

Co-occurrences

#ZygosityAllelesNumber of Observations
1SingleHeterozygoteBRCA1:5697insC1

From Breast Cancer Information Core (BIC) (BRCA1), SCV000145293.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided6not providednot providedclinical testingnot provided
2African1not providednot providedclinical testingnot provided
3African American1not providednot providedclinical testingnot provided
4Latin American, Caribbean1not providednot providedclinical testingnot provided
5Western European2not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided6not providednot providednot provided
2germlineyesnot providednot providednot provided1not providednot providednot provided
3germlineyesnot providednot providednot provided1not providednot providednot provided
4germlineyesnot providednot providednot provided1not providednot providednot provided
5germlineyesnot providednot providednot provided2not providednot providednot provided

From Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), c/o University of Cambridge, SCV000326135.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot provided7not provided

From Brotman Baty Institute, University of Washington, SCV001244020.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedin vitro PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1not applicablenot applicablenot providednot providednot providednot providednot providednot providednot provided

From MGZ Medical Genetics Center, SCV002578917.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

From St. Jude Molecular Pathology, St. Jude Children's Research Hospital, SCV003843144.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The BRCA1 c.5074G>A (p.Asp1692Asn) missense change affects the last nucleotide of exon 16 and is predicted to abolish the native splice donor site. An in vitro study demonstrated that this variant leads to multiple aberrant transcripts, including one causing exon 17 skipping and another causing activation of a cryptic splice donor site that leads to an in-frame retention of 153 bp of intron 17 (PMID: 25724305). These published findings are also supported by internal data. This variant has been reported in individuals with a personal and/or family history of breast and/or ovarian cancer (PMID: 8460636, 9452084, 10196379, 15571962). It is commonly reported in individuals of Icelandic ancestry and genetic linkage analysis suggests that this is an Icelandic founder mutation (PMID: 8460636, 9452084, 15571962). It is absent in gnomAD v2.1.1 (https://gnomad.broadinstitute.org/). In summary, this variant meets criteria to be classified as likely pathogenic.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From deCODE genetics, Amgen, SCV004022171.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1Icelandic70not providednot providedresearchnot provided

Description

The variant NM_007294.4:c.5074G>A (chr17:43067608) in BRCA1 was detected in 26 heterozygotes out of 58K WGS Icelanders (MAF= 0,022%). Following imputation in a set of 166K Icelanders (70 imputed heterozygotes) we observed an association with breast cancer using 6908 cases and 292623 controls (OR= 20.57, P= 8.44e-16) and ovarian cancer using 907 cases and 299709 controls (OR= 29.05, P= 2.67e-10). This variant has been reported in ClinVar previously as pathogenic/likely pathogenic. Based on ACMG criteria (PS4, PP1, PP3, PP5_Strong) this variant classifies as pathogenic.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided70not providednot providednot provided

From Department of Medical and Surgical Sciences, University of Bologna, SCV004228368.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

PS3(Strong)+PM2(Supporting)+PP3(Supporting)+PP4(Supporting) according to ACMG/AMP classification guidelines specified for BRCA1 & BRCA2 (Classification Criteria V1.0.0 2023-09-08 - https://cspec.genome.network/cspec/ui/svi/affiliation/50087) (PMID: 38160042)

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Apr 28, 2025