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 starscriteria provided, multiple submitters, no conflicts
- Somatic classification
of clinical impact: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Somatic classification
of oncogenicity: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno 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
This HGVS expression did not pass validation- 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)
- The saturation genome editing (SGE) assay for BRCA1 NM_007294.3:c.5074G>A, a MISSENSE variant, produced a function score of -1.86, corresponding to a functional classification of LOSS_OF_FUNCTION. SGE function score ranges for classification are as follows: ‘functional’, score > -0.748; ‘intermediate’, -0.748 > score > -1.328; ‘non-functional’, score < -1.328. The median synonymous SNV scored 0.0 and the median nonsense SNV scored -2.12.
- Observations:
- 7
Condition(s)
Assertion and evidence details
Submission Accession | Submitter | Review Status (Assertion method) | Clinical Significance (Last evaluated) | Origin | Method | Citations |
---|---|---|---|---|---|---|
SCV000053813 | Sharing Clinical Reports Project (SCRP) | no assertion criteria provided | Likely pathogenic (Jul 25, 2006) | germline | clinical testing | |
SCV000145293 | Breast Cancer Information Core (BIC) (BRCA1) | no assertion criteria provided | Pathogenic (May 29, 2002) | germline | clinical testing | |
SCV000326135 | Consortium 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) | germline | clinical testing | CIMBA_Mutation_Classification_guidelines_May16.pdf, |
SCV001244020 | Brotman Baty Institute, University of Washington | no classification provided | not provided | not applicable | in vitro | |
SCV002578917 | MGZ Medical Genetics Center | criteria provided, single submitter (ACMG Guidelines, 2015) | Pathogenic (May 20, 2022) | germline | clinical testing | |
SCV003843144 | St. Jude Molecular Pathology, St. Jude Children's Research Hospital | criteria provided, single submitter (St. Jude Assertion Criteria 2020) | Likely pathogenic (Nov 4, 2022) | germline | clinical testing | |
SCV004022171 | deCODE genetics, Amgen | no assertion criteria provided | Pathogenic (Jul 21, 2023) | germline | research | |
SCV004228368 | Department of Medical and Surgical Sciences, University of Bologna | no assertion criteria provided | Likely pathogenic (Sep 1, 2023) | germline | clinical testing |
Summary from all submissions
Ethnicity | Origin | Affected | Individuals | Families | Chromosomes tested | Number Tested | Family history | Method |
---|---|---|---|---|---|---|---|---|
not provided | germline | yes | 7 | not provided | not provided | not provided | not provided | clinical testing |
not provided | germline | unknown | not provided | 7 | not provided | not provided | not provided | clinical testing |
not provided | germline | not provided | 1 | not provided | not provided | 1 | not provided | clinical testing |
not provided | not applicable | not applicable | not provided | not provided | not provided | not provided | not provided | in vitro |
African | germline | yes | 1 | not provided | not provided | not provided | not provided | clinical testing |
African American | germline | yes | 1 | not provided | not provided | not provided | not provided | clinical testing |
Icelandic | germline | yes | 70 | not provided | not provided | not provided | not provided | research |
Latin American, Caribbean | germline | yes | 1 | not provided | not provided | not provided | not provided | clinical testing |
Western European | germline | yes | 2 | not provided | not provided | not provided | not provided | clinical 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.
- PMID:
- 30209399
- PMCID:
- PMC6181777
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.
- PMID:
- 25741868
- PMCID:
- PMC4544753
Details of each submission
From Sharing Clinical Reports Project (SCRP), SCV000053813.5
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | not provided |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | not provided | 1 | not provided | not provided | not provided | not provided | not provided | See 1 |
Co-occurrences
# | Zygosity | Alleles | Number of Observations |
---|---|---|---|
1 | SingleHeterozygote | BRCA1:5697insC | 1 |
From Breast Cancer Information Core (BIC) (BRCA1), SCV000145293.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | 6 | not provided | not provided | clinical testing | not provided |
2 | African | 1 | not provided | not provided | clinical testing | not provided |
3 | African American | 1 | not provided | not provided | clinical testing | not provided |
4 | Latin American, Caribbean | 1 | not provided | not provided | clinical testing | not provided |
5 | Western European | 2 | not provided | not provided | clinical testing | not provided |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | yes | not provided | not provided | not provided | 6 | not provided | not provided | not provided | |
2 | germline | yes | not provided | not provided | not provided | 1 | not provided | not provided | not provided | |
3 | germline | yes | not provided | not provided | not provided | 1 | not provided | not provided | not provided | |
4 | germline | yes | not provided | not provided | not provided | 1 | not provided | not provided | not provided | |
5 | germline | yes | not provided | not provided | not provided | 2 | not provided | not provided | not provided |
From Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), c/o University of Cambridge, SCV000326135.4
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | not provided |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | unknown | not provided | not provided | not provided | not provided | not provided | 7 | not provided |
From Brotman Baty Institute, University of Washington, SCV001244020.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | in vitro | PubMed (1) |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | not applicable | not applicable | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
From MGZ Medical Genetics Center, SCV002578917.2
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | 1 | not provided | not provided | clinical testing | PubMed (1) |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | yes | not provided | not provided | not provided | 1 | not provided | not provided | not provided |
From St. Jude Molecular Pathology, St. Jude Children's Research Hospital, SCV003843144.2
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | not 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.
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | unknown | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
From deCODE genetics, Amgen, SCV004022171.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | Icelandic | 70 | not provided | not provided | research | not 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.
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | yes | not provided | not provided | not provided | 70 | not provided | not provided | not provided |
From Department of Medical and Surgical Sciences, University of Bologna, SCV004228368.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | not 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)
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | yes | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
Last Updated: Apr 28, 2025