U.S. flag

An official website of the United States government

NM_007294.4(BRCA1):c.1256T>G (p.Val419Gly) AND Hereditary cancer-predisposing syndrome

Germline classification:
Conflicting interpretations of pathogenicity (2 submissions)
Last evaluated:
Jun 30, 2023
Review status:
criteria provided, conflicting classifications
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:
RCV001010363.16

Allele description [Variation Report for NM_007294.4(BRCA1):c.1256T>G (p.Val419Gly)]

NM_007294.4(BRCA1):c.1256T>G (p.Val419Gly)

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.1256T>G (p.Val419Gly)
HGVS:
  • NC_000017.11:g.43094275A>C
  • NG_005905.2:g.123709T>G
  • NM_001407571.1:c.1043T>G
  • NM_001407581.1:c.1256T>G
  • NM_001407582.1:c.1256T>G
  • NM_001407583.1:c.1256T>G
  • NM_001407585.1:c.1256T>G
  • NM_001407587.1:c.1253T>G
  • NM_001407590.1:c.1253T>G
  • NM_001407591.1:c.1253T>G
  • NM_001407593.1:c.1256T>G
  • NM_001407594.1:c.1256T>G
  • NM_001407596.1:c.1256T>G
  • NM_001407597.1:c.1256T>G
  • NM_001407598.1:c.1256T>G
  • NM_001407602.1:c.1256T>G
  • NM_001407603.1:c.1256T>G
  • NM_001407605.1:c.1256T>G
  • NM_001407610.1:c.1253T>G
  • NM_001407611.1:c.1253T>G
  • NM_001407612.1:c.1253T>G
  • NM_001407613.1:c.1253T>G
  • NM_001407614.1:c.1253T>G
  • NM_001407615.1:c.1253T>G
  • NM_001407616.1:c.1256T>G
  • NM_001407617.1:c.1256T>G
  • NM_001407618.1:c.1256T>G
  • NM_001407619.1:c.1256T>G
  • NM_001407620.1:c.1256T>G
  • NM_001407621.1:c.1256T>G
  • NM_001407622.1:c.1256T>G
  • NM_001407623.1:c.1256T>G
  • NM_001407624.1:c.1256T>G
  • NM_001407625.1:c.1256T>G
  • NM_001407626.1:c.1256T>G
  • NM_001407627.1:c.1253T>G
  • NM_001407628.1:c.1253T>G
  • NM_001407629.1:c.1253T>G
  • NM_001407630.1:c.1253T>G
  • NM_001407631.1:c.1253T>G
  • NM_001407632.1:c.1253T>G
  • NM_001407633.1:c.1253T>G
  • NM_001407634.1:c.1253T>G
  • NM_001407635.1:c.1253T>G
  • NM_001407636.1:c.1253T>G
  • NM_001407637.1:c.1253T>G
  • NM_001407638.1:c.1253T>G
  • NM_001407639.1:c.1256T>G
  • NM_001407640.1:c.1256T>G
  • NM_001407641.1:c.1256T>G
  • NM_001407642.1:c.1256T>G
  • NM_001407644.1:c.1253T>G
  • NM_001407645.1:c.1253T>G
  • NM_001407646.1:c.1247T>G
  • NM_001407647.1:c.1247T>G
  • NM_001407648.1:c.1133T>G
  • NM_001407649.1:c.1130T>G
  • NM_001407652.1:c.1256T>G
  • NM_001407653.1:c.1178T>G
  • NM_001407654.1:c.1178T>G
  • NM_001407655.1:c.1178T>G
  • NM_001407656.1:c.1178T>G
  • NM_001407657.1:c.1178T>G
  • NM_001407658.1:c.1178T>G
  • NM_001407659.1:c.1175T>G
  • NM_001407660.1:c.1175T>G
  • NM_001407661.1:c.1175T>G
  • NM_001407662.1:c.1175T>G
  • NM_001407663.1:c.1178T>G
  • NM_001407664.1:c.1133T>G
  • NM_001407665.1:c.1133T>G
  • NM_001407666.1:c.1133T>G
  • NM_001407667.1:c.1133T>G
  • NM_001407668.1:c.1133T>G
  • NM_001407669.1:c.1133T>G
  • NM_001407670.1:c.1130T>G
  • NM_001407671.1:c.1130T>G
  • NM_001407672.1:c.1130T>G
  • NM_001407673.1:c.1130T>G
  • NM_001407674.1:c.1133T>G
  • NM_001407675.1:c.1133T>G
  • NM_001407676.1:c.1133T>G
  • NM_001407677.1:c.1133T>G
  • NM_001407678.1:c.1133T>G
  • NM_001407679.1:c.1133T>G
  • NM_001407680.1:c.1133T>G
  • NM_001407681.1:c.1133T>G
  • NM_001407682.1:c.1133T>G
  • NM_001407683.1:c.1133T>G
  • NM_001407684.1:c.1256T>G
  • NM_001407685.1:c.1130T>G
  • NM_001407686.1:c.1130T>G
  • NM_001407687.1:c.1130T>G
  • NM_001407688.1:c.1130T>G
  • NM_001407689.1:c.1130T>G
  • NM_001407690.1:c.1130T>G
  • NM_001407691.1:c.1130T>G
  • NM_001407692.1:c.1115T>G
  • NM_001407694.1:c.1115T>G
  • NM_001407695.1:c.1115T>G
  • NM_001407696.1:c.1115T>G
  • NM_001407697.1:c.1115T>G
  • NM_001407698.1:c.1115T>G
  • NM_001407724.1:c.1115T>G
  • NM_001407725.1:c.1115T>G
  • NM_001407726.1:c.1115T>G
  • NM_001407727.1:c.1115T>G
  • NM_001407728.1:c.1115T>G
  • NM_001407729.1:c.1115T>G
  • NM_001407730.1:c.1115T>G
  • NM_001407731.1:c.1115T>G
  • NM_001407732.1:c.1115T>G
  • NM_001407733.1:c.1115T>G
  • NM_001407734.1:c.1115T>G
  • NM_001407735.1:c.1115T>G
  • NM_001407736.1:c.1115T>G
  • NM_001407737.1:c.1115T>G
  • NM_001407738.1:c.1115T>G
  • NM_001407739.1:c.1115T>G
  • NM_001407740.1:c.1112T>G
  • NM_001407741.1:c.1112T>G
  • NM_001407742.1:c.1112T>G
  • NM_001407743.1:c.1112T>G
  • NM_001407744.1:c.1112T>G
  • NM_001407745.1:c.1112T>G
  • NM_001407746.1:c.1112T>G
  • NM_001407747.1:c.1112T>G
  • NM_001407748.1:c.1112T>G
  • NM_001407749.1:c.1112T>G
  • NM_001407750.1:c.1115T>G
  • NM_001407751.1:c.1115T>G
  • NM_001407752.1:c.1115T>G
  • NM_001407838.1:c.1112T>G
  • NM_001407839.1:c.1112T>G
  • NM_001407841.1:c.1112T>G
  • NM_001407842.1:c.1112T>G
  • NM_001407843.1:c.1112T>G
  • NM_001407844.1:c.1112T>G
  • NM_001407845.1:c.1112T>G
  • NM_001407846.1:c.1112T>G
  • NM_001407847.1:c.1112T>G
  • NM_001407848.1:c.1112T>G
  • NM_001407849.1:c.1112T>G
  • NM_001407850.1:c.1115T>G
  • NM_001407851.1:c.1115T>G
  • NM_001407852.1:c.1115T>G
  • NM_001407853.1:c.1043T>G
  • NM_001407854.1:c.1256T>G
  • NM_001407858.1:c.1256T>G
  • NM_001407859.1:c.1256T>G
  • NM_001407860.1:c.1253T>G
  • NM_001407861.1:c.1253T>G
  • NM_001407862.1:c.1055T>G
  • NM_001407863.1:c.1133T>G
  • NM_001407874.1:c.1052T>G
  • NM_001407875.1:c.1052T>G
  • NM_001407879.1:c.1046T>G
  • NM_001407881.1:c.1046T>G
  • NM_001407882.1:c.1046T>G
  • NM_001407884.1:c.1046T>G
  • NM_001407885.1:c.1046T>G
  • NM_001407886.1:c.1046T>G
  • NM_001407887.1:c.1046T>G
  • NM_001407889.1:c.1046T>G
  • NM_001407894.1:c.1043T>G
  • NM_001407895.1:c.1043T>G
  • NM_001407896.1:c.1043T>G
  • NM_001407897.1:c.1043T>G
  • NM_001407898.1:c.1043T>G
  • NM_001407899.1:c.1043T>G
  • NM_001407900.1:c.1046T>G
  • NM_001407902.1:c.1046T>G
  • NM_001407904.1:c.1046T>G
  • NM_001407906.1:c.1046T>G
  • NM_001407907.1:c.1046T>G
  • NM_001407908.1:c.1046T>G
  • NM_001407909.1:c.1046T>G
  • NM_001407910.1:c.1046T>G
  • NM_001407915.1:c.1043T>G
  • NM_001407916.1:c.1043T>G
  • NM_001407917.1:c.1043T>G
  • NM_001407918.1:c.1043T>G
  • NM_001407919.1:c.1133T>G
  • NM_001407920.1:c.992T>G
  • NM_001407921.1:c.992T>G
  • NM_001407922.1:c.992T>G
  • NM_001407923.1:c.992T>G
  • NM_001407924.1:c.992T>G
  • NM_001407925.1:c.992T>G
  • NM_001407926.1:c.992T>G
  • NM_001407927.1:c.992T>G
  • NM_001407928.1:c.992T>G
  • NM_001407929.1:c.992T>G
  • NM_001407930.1:c.989T>G
  • NM_001407931.1:c.989T>G
  • NM_001407932.1:c.989T>G
  • NM_001407933.1:c.992T>G
  • NM_001407934.1:c.989T>G
  • NM_001407935.1:c.992T>G
  • NM_001407936.1:c.989T>G
  • NM_001407937.1:c.1133T>G
  • NM_001407938.1:c.1133T>G
  • NM_001407939.1:c.1133T>G
  • NM_001407940.1:c.1130T>G
  • NM_001407941.1:c.1130T>G
  • NM_001407942.1:c.1115T>G
  • NM_001407943.1:c.1112T>G
  • NM_001407944.1:c.1115T>G
  • NM_001407945.1:c.1115T>G
  • NM_001407946.1:c.923T>G
  • NM_001407947.1:c.923T>G
  • NM_001407948.1:c.923T>G
  • NM_001407949.1:c.923T>G
  • NM_001407950.1:c.923T>G
  • NM_001407951.1:c.923T>G
  • NM_001407952.1:c.923T>G
  • NM_001407953.1:c.923T>G
  • NM_001407954.1:c.920T>G
  • NM_001407955.1:c.920T>G
  • NM_001407956.1:c.920T>G
  • NM_001407957.1:c.923T>G
  • NM_001407958.1:c.920T>G
  • NM_001407959.1:c.875T>G
  • NM_001407960.1:c.875T>G
  • NM_001407962.1:c.872T>G
  • NM_001407963.1:c.875T>G
  • NM_001407964.1:c.1112T>G
  • NM_001407965.1:c.752T>G
  • NM_001407966.1:c.368T>G
  • NM_001407967.1:c.368T>G
  • NM_001407968.1:c.787+469T>G
  • NM_001407969.1:c.787+469T>G
  • NM_001407970.1:c.787+469T>G
  • NM_001407971.1:c.787+469T>G
  • NM_001407972.1:c.784+469T>G
  • NM_001407973.1:c.787+469T>G
  • NM_001407974.1:c.787+469T>G
  • NM_001407975.1:c.787+469T>G
  • NM_001407976.1:c.787+469T>G
  • NM_001407977.1:c.787+469T>G
  • NM_001407978.1:c.787+469T>G
  • NM_001407979.1:c.787+469T>G
  • NM_001407980.1:c.787+469T>G
  • NM_001407981.1:c.787+469T>G
  • NM_001407982.1:c.787+469T>G
  • NM_001407983.1:c.787+469T>G
  • NM_001407984.1:c.784+469T>G
  • NM_001407985.1:c.784+469T>G
  • NM_001407986.1:c.784+469T>G
  • NM_001407990.1:c.787+469T>G
  • NM_001407991.1:c.784+469T>G
  • NM_001407992.1:c.784+469T>G
  • NM_001407993.1:c.787+469T>G
  • NM_001408392.1:c.784+469T>G
  • NM_001408396.1:c.784+469T>G
  • NM_001408397.1:c.784+469T>G
  • NM_001408398.1:c.784+469T>G
  • NM_001408399.1:c.784+469T>G
  • NM_001408400.1:c.784+469T>G
  • NM_001408401.1:c.784+469T>G
  • NM_001408402.1:c.784+469T>G
  • NM_001408403.1:c.787+469T>G
  • NM_001408404.1:c.787+469T>G
  • NM_001408406.1:c.790+466T>G
  • NM_001408407.1:c.784+469T>G
  • NM_001408408.1:c.778+469T>G
  • NM_001408409.1:c.709+469T>G
  • NM_001408410.1:c.646+469T>G
  • NM_001408411.1:c.709+469T>G
  • NM_001408412.1:c.709+469T>G
  • NM_001408413.1:c.706+469T>G
  • NM_001408414.1:c.709+469T>G
  • NM_001408415.1:c.709+469T>G
  • NM_001408416.1:c.706+469T>G
  • NM_001408418.1:c.670+1571T>G
  • NM_001408419.1:c.670+1571T>G
  • NM_001408420.1:c.670+1571T>G
  • NM_001408421.1:c.667+1571T>G
  • NM_001408422.1:c.670+1571T>G
  • NM_001408423.1:c.670+1571T>G
  • NM_001408424.1:c.667+1571T>G
  • NM_001408425.1:c.664+469T>G
  • NM_001408426.1:c.664+469T>G
  • NM_001408427.1:c.664+469T>G
  • NM_001408428.1:c.664+469T>G
  • NM_001408429.1:c.664+469T>G
  • NM_001408430.1:c.664+469T>G
  • NM_001408431.1:c.667+1571T>G
  • NM_001408432.1:c.661+469T>G
  • NM_001408433.1:c.661+469T>G
  • NM_001408434.1:c.661+469T>G
  • NM_001408435.1:c.661+469T>G
  • NM_001408436.1:c.664+469T>G
  • NM_001408437.1:c.664+469T>G
  • NM_001408438.1:c.664+469T>G
  • NM_001408439.1:c.664+469T>G
  • NM_001408440.1:c.664+469T>G
  • NM_001408441.1:c.664+469T>G
  • NM_001408442.1:c.664+469T>G
  • NM_001408443.1:c.664+469T>G
  • NM_001408444.1:c.664+469T>G
  • NM_001408445.1:c.661+469T>G
  • NM_001408446.1:c.661+469T>G
  • NM_001408447.1:c.661+469T>G
  • NM_001408448.1:c.661+469T>G
  • NM_001408450.1:c.661+469T>G
  • NM_001408451.1:c.652+469T>G
  • NM_001408452.1:c.646+469T>G
  • NM_001408453.1:c.646+469T>G
  • NM_001408454.1:c.646+469T>G
  • NM_001408455.1:c.646+469T>G
  • NM_001408456.1:c.646+469T>G
  • NM_001408457.1:c.646+469T>G
  • NM_001408458.1:c.646+469T>G
  • NM_001408459.1:c.646+469T>G
  • NM_001408460.1:c.646+469T>G
  • NM_001408461.1:c.646+469T>G
  • NM_001408462.1:c.643+469T>G
  • NM_001408463.1:c.643+469T>G
  • NM_001408464.1:c.643+469T>G
  • NM_001408465.1:c.643+469T>G
  • NM_001408466.1:c.646+469T>G
  • NM_001408467.1:c.646+469T>G
  • NM_001408468.1:c.643+469T>G
  • NM_001408469.1:c.646+469T>G
  • NM_001408470.1:c.643+469T>G
  • NM_001408472.1:c.787+469T>G
  • NM_001408473.1:c.784+469T>G
  • NM_001408474.1:c.586+469T>G
  • NM_001408475.1:c.583+469T>G
  • NM_001408476.1:c.586+469T>G
  • NM_001408478.1:c.577+469T>G
  • NM_001408479.1:c.577+469T>G
  • NM_001408480.1:c.577+469T>G
  • NM_001408481.1:c.577+469T>G
  • NM_001408482.1:c.577+469T>G
  • NM_001408483.1:c.577+469T>G
  • NM_001408484.1:c.577+469T>G
  • NM_001408485.1:c.577+469T>G
  • NM_001408489.1:c.577+469T>G
  • NM_001408490.1:c.574+469T>G
  • NM_001408491.1:c.574+469T>G
  • NM_001408492.1:c.577+469T>G
  • NM_001408493.1:c.574+469T>G
  • NM_001408494.1:c.548-3243T>G
  • NM_001408495.1:c.545-3243T>G
  • NM_001408496.1:c.523+469T>G
  • NM_001408497.1:c.523+469T>G
  • NM_001408498.1:c.523+469T>G
  • NM_001408499.1:c.523+469T>G
  • NM_001408500.1:c.523+469T>G
  • NM_001408501.1:c.523+469T>G
  • NM_001408502.1:c.454+469T>G
  • NM_001408503.1:c.520+469T>G
  • NM_001408504.1:c.520+469T>G
  • NM_001408505.1:c.520+469T>G
  • NM_001408506.1:c.460+1571T>G
  • NM_001408507.1:c.460+1571T>G
  • NM_001408508.1:c.451+469T>G
  • NM_001408509.1:c.451+469T>G
  • NM_001408510.1:c.406+469T>G
  • NM_001408511.1:c.404-3243T>G
  • NM_001408512.1:c.283+469T>G
  • NM_001408513.1:c.577+469T>G
  • NM_001408514.1:c.577+469T>G
  • NM_007294.4:c.1256T>GMANE SELECT
  • NM_007297.4:c.1115T>G
  • NM_007298.4:c.787+469T>G
  • NM_007299.4:c.787+469T>G
  • NM_007300.4:c.1256T>G
  • NP_001394500.1:p.Val348Gly
  • NP_001394510.1:p.Val419Gly
  • NP_001394511.1:p.Val419Gly
  • NP_001394512.1:p.Val419Gly
  • NP_001394514.1:p.Val419Gly
  • NP_001394516.1:p.Val418Gly
  • NP_001394519.1:p.Val418Gly
  • NP_001394520.1:p.Val418Gly
  • NP_001394522.1:p.Val419Gly
  • NP_001394523.1:p.Val419Gly
  • NP_001394525.1:p.Val419Gly
  • NP_001394526.1:p.Val419Gly
  • NP_001394527.1:p.Val419Gly
  • NP_001394531.1:p.Val419Gly
  • NP_001394532.1:p.Val419Gly
  • NP_001394534.1:p.Val419Gly
  • NP_001394539.1:p.Val418Gly
  • NP_001394540.1:p.Val418Gly
  • NP_001394541.1:p.Val418Gly
  • NP_001394542.1:p.Val418Gly
  • NP_001394543.1:p.Val418Gly
  • NP_001394544.1:p.Val418Gly
  • NP_001394545.1:p.Val419Gly
  • NP_001394546.1:p.Val419Gly
  • NP_001394547.1:p.Val419Gly
  • NP_001394548.1:p.Val419Gly
  • NP_001394549.1:p.Val419Gly
  • NP_001394550.1:p.Val419Gly
  • NP_001394551.1:p.Val419Gly
  • NP_001394552.1:p.Val419Gly
  • NP_001394553.1:p.Val419Gly
  • NP_001394554.1:p.Val419Gly
  • NP_001394555.1:p.Val419Gly
  • NP_001394556.1:p.Val418Gly
  • NP_001394557.1:p.Val418Gly
  • NP_001394558.1:p.Val418Gly
  • NP_001394559.1:p.Val418Gly
  • NP_001394560.1:p.Val418Gly
  • NP_001394561.1:p.Val418Gly
  • NP_001394562.1:p.Val418Gly
  • NP_001394563.1:p.Val418Gly
  • NP_001394564.1:p.Val418Gly
  • NP_001394565.1:p.Val418Gly
  • NP_001394566.1:p.Val418Gly
  • NP_001394567.1:p.Val418Gly
  • NP_001394568.1:p.Val419Gly
  • NP_001394569.1:p.Val419Gly
  • NP_001394570.1:p.Val419Gly
  • NP_001394571.1:p.Val419Gly
  • NP_001394573.1:p.Val418Gly
  • NP_001394574.1:p.Val418Gly
  • NP_001394575.1:p.Val416Gly
  • NP_001394576.1:p.Val416Gly
  • NP_001394577.1:p.Val378Gly
  • NP_001394578.1:p.Val377Gly
  • NP_001394581.1:p.Val419Gly
  • NP_001394582.1:p.Val393Gly
  • NP_001394583.1:p.Val393Gly
  • NP_001394584.1:p.Val393Gly
  • NP_001394585.1:p.Val393Gly
  • NP_001394586.1:p.Val393Gly
  • NP_001394587.1:p.Val393Gly
  • NP_001394588.1:p.Val392Gly
  • NP_001394589.1:p.Val392Gly
  • NP_001394590.1:p.Val392Gly
  • NP_001394591.1:p.Val392Gly
  • NP_001394592.1:p.Val393Gly
  • NP_001394593.1:p.Val378Gly
  • NP_001394594.1:p.Val378Gly
  • NP_001394595.1:p.Val378Gly
  • NP_001394596.1:p.Val378Gly
  • NP_001394597.1:p.Val378Gly
  • NP_001394598.1:p.Val378Gly
  • NP_001394599.1:p.Val377Gly
  • NP_001394600.1:p.Val377Gly
  • NP_001394601.1:p.Val377Gly
  • NP_001394602.1:p.Val377Gly
  • NP_001394603.1:p.Val378Gly
  • NP_001394604.1:p.Val378Gly
  • NP_001394605.1:p.Val378Gly
  • NP_001394606.1:p.Val378Gly
  • NP_001394607.1:p.Val378Gly
  • NP_001394608.1:p.Val378Gly
  • NP_001394609.1:p.Val378Gly
  • NP_001394610.1:p.Val378Gly
  • NP_001394611.1:p.Val378Gly
  • NP_001394612.1:p.Val378Gly
  • NP_001394613.1:p.Val419Gly
  • NP_001394614.1:p.Val377Gly
  • NP_001394615.1:p.Val377Gly
  • NP_001394616.1:p.Val377Gly
  • NP_001394617.1:p.Val377Gly
  • NP_001394618.1:p.Val377Gly
  • NP_001394619.1:p.Val377Gly
  • NP_001394620.1:p.Val377Gly
  • NP_001394621.1:p.Val372Gly
  • NP_001394623.1:p.Val372Gly
  • NP_001394624.1:p.Val372Gly
  • NP_001394625.1:p.Val372Gly
  • NP_001394626.1:p.Val372Gly
  • NP_001394627.1:p.Val372Gly
  • NP_001394653.1:p.Val372Gly
  • NP_001394654.1:p.Val372Gly
  • NP_001394655.1:p.Val372Gly
  • NP_001394656.1:p.Val372Gly
  • NP_001394657.1:p.Val372Gly
  • NP_001394658.1:p.Val372Gly
  • NP_001394659.1:p.Val372Gly
  • NP_001394660.1:p.Val372Gly
  • NP_001394661.1:p.Val372Gly
  • NP_001394662.1:p.Val372Gly
  • NP_001394663.1:p.Val372Gly
  • NP_001394664.1:p.Val372Gly
  • NP_001394665.1:p.Val372Gly
  • NP_001394666.1:p.Val372Gly
  • NP_001394667.1:p.Val372Gly
  • NP_001394668.1:p.Val372Gly
  • NP_001394669.1:p.Val371Gly
  • NP_001394670.1:p.Val371Gly
  • NP_001394671.1:p.Val371Gly
  • NP_001394672.1:p.Val371Gly
  • NP_001394673.1:p.Val371Gly
  • NP_001394674.1:p.Val371Gly
  • NP_001394675.1:p.Val371Gly
  • NP_001394676.1:p.Val371Gly
  • NP_001394677.1:p.Val371Gly
  • NP_001394678.1:p.Val371Gly
  • NP_001394679.1:p.Val372Gly
  • NP_001394680.1:p.Val372Gly
  • NP_001394681.1:p.Val372Gly
  • NP_001394767.1:p.Val371Gly
  • NP_001394768.1:p.Val371Gly
  • NP_001394770.1:p.Val371Gly
  • NP_001394771.1:p.Val371Gly
  • NP_001394772.1:p.Val371Gly
  • NP_001394773.1:p.Val371Gly
  • NP_001394774.1:p.Val371Gly
  • NP_001394775.1:p.Val371Gly
  • NP_001394776.1:p.Val371Gly
  • NP_001394777.1:p.Val371Gly
  • NP_001394778.1:p.Val371Gly
  • NP_001394779.1:p.Val372Gly
  • NP_001394780.1:p.Val372Gly
  • NP_001394781.1:p.Val372Gly
  • NP_001394782.1:p.Val348Gly
  • NP_001394783.1:p.Val419Gly
  • NP_001394787.1:p.Val419Gly
  • NP_001394788.1:p.Val419Gly
  • NP_001394789.1:p.Val418Gly
  • NP_001394790.1:p.Val418Gly
  • NP_001394791.1:p.Val352Gly
  • NP_001394792.1:p.Val378Gly
  • NP_001394803.1:p.Val351Gly
  • NP_001394804.1:p.Val351Gly
  • NP_001394808.1:p.Val349Gly
  • NP_001394810.1:p.Val349Gly
  • NP_001394811.1:p.Val349Gly
  • NP_001394813.1:p.Val349Gly
  • NP_001394814.1:p.Val349Gly
  • NP_001394815.1:p.Val349Gly
  • NP_001394816.1:p.Val349Gly
  • NP_001394818.1:p.Val349Gly
  • NP_001394823.1:p.Val348Gly
  • NP_001394824.1:p.Val348Gly
  • NP_001394825.1:p.Val348Gly
  • NP_001394826.1:p.Val348Gly
  • NP_001394827.1:p.Val348Gly
  • NP_001394828.1:p.Val348Gly
  • NP_001394829.1:p.Val349Gly
  • NP_001394831.1:p.Val349Gly
  • NP_001394833.1:p.Val349Gly
  • NP_001394835.1:p.Val349Gly
  • NP_001394836.1:p.Val349Gly
  • NP_001394837.1:p.Val349Gly
  • NP_001394838.1:p.Val349Gly
  • NP_001394839.1:p.Val349Gly
  • NP_001394844.1:p.Val348Gly
  • NP_001394845.1:p.Val348Gly
  • NP_001394846.1:p.Val348Gly
  • NP_001394847.1:p.Val348Gly
  • NP_001394848.1:p.Val378Gly
  • NP_001394849.1:p.Val331Gly
  • NP_001394850.1:p.Val331Gly
  • NP_001394851.1:p.Val331Gly
  • NP_001394852.1:p.Val331Gly
  • NP_001394853.1:p.Val331Gly
  • NP_001394854.1:p.Val331Gly
  • NP_001394855.1:p.Val331Gly
  • NP_001394856.1:p.Val331Gly
  • NP_001394857.1:p.Val331Gly
  • NP_001394858.1:p.Val331Gly
  • NP_001394859.1:p.Val330Gly
  • NP_001394860.1:p.Val330Gly
  • NP_001394861.1:p.Val330Gly
  • NP_001394862.1:p.Val331Gly
  • NP_001394863.1:p.Val330Gly
  • NP_001394864.1:p.Val331Gly
  • NP_001394865.1:p.Val330Gly
  • NP_001394866.1:p.Val378Gly
  • NP_001394867.1:p.Val378Gly
  • NP_001394868.1:p.Val378Gly
  • NP_001394869.1:p.Val377Gly
  • NP_001394870.1:p.Val377Gly
  • NP_001394871.1:p.Val372Gly
  • NP_001394872.1:p.Val371Gly
  • NP_001394873.1:p.Val372Gly
  • NP_001394874.1:p.Val372Gly
  • NP_001394875.1:p.Val308Gly
  • NP_001394876.1:p.Val308Gly
  • NP_001394877.1:p.Val308Gly
  • NP_001394878.1:p.Val308Gly
  • NP_001394879.1:p.Val308Gly
  • NP_001394880.1:p.Val308Gly
  • NP_001394881.1:p.Val308Gly
  • NP_001394882.1:p.Val308Gly
  • NP_001394883.1:p.Val307Gly
  • NP_001394884.1:p.Val307Gly
  • NP_001394885.1:p.Val307Gly
  • NP_001394886.1:p.Val308Gly
  • NP_001394887.1:p.Val307Gly
  • NP_001394888.1:p.Val292Gly
  • NP_001394889.1:p.Val292Gly
  • NP_001394891.1:p.Val291Gly
  • NP_001394892.1:p.Val292Gly
  • NP_001394893.1:p.Val371Gly
  • NP_001394894.1:p.Val251Gly
  • NP_001394895.1:p.Val123Gly
  • NP_001394896.1:p.Val123Gly
  • NP_009225.1:p.Val419Gly
  • NP_009225.1:p.Val419Gly
  • NP_009228.2:p.Val372Gly
  • NP_009231.2:p.Val419Gly
  • LRG_292t1:c.1256T>G
  • LRG_292:g.123709T>G
  • LRG_292p1:p.Val419Gly
  • NC_000017.10:g.41246292A>C
  • NM_007294.3:c.1256T>G
  • NR_027676.1:n.1392T>G
Nucleotide change:
1375T>G
Protein change:
V123G
Links:
dbSNP: rs398122628
NCBI 1000 Genomes Browser:
rs398122628
Molecular consequence:
  • NM_001407968.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.790+466T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.778+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.709+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.709+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.709+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.706+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.709+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.709+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.706+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.670+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.670+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.670+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.667+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.670+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.670+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.667+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.667+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.661+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.661+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.661+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.661+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.664+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.661+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.661+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.661+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.661+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.661+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.652+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.643+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.643+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.643+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.643+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.643+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.646+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.643+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.784+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.586+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.583+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.586+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.574+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.574+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.574+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.548-3243T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.545-3243T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.523+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.523+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.523+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.523+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.523+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.523+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.454+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.520+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.520+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.520+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.460+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.460+1571T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.451+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.451+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.406+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.404-3243T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.283+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.577+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.787+469T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.1247T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.1247T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.1178T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.1178T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.1178T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.1178T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.1178T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.1178T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.1175T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.1175T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.1175T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.1175T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.1178T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.1253T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.1055T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.1052T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.1052T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.1046T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.1043T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.989T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.989T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.989T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.989T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.992T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.989T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.1133T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.1130T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.923T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.923T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.923T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.923T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.923T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.923T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.923T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.923T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.920T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.920T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.920T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.923T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.920T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.875T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.875T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.872T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.875T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.1112T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.752T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.368T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.368T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.1115T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.1256T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001170550Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Jun 30, 2023) 		germlineclinical testing

Citation Link,

SCV003846067University of Washington Department of Laboratory Medicine, University of Washington
criteria provided, single submitter

(Dines et al. (Genet Med. 2020))		Likely benign
(Mar 23, 2023) 		germlinecuration

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing, curation

Citations

PubMed

Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots".

Dines JN, Shirts BH, Slavin TP, Walsh T, King MC, Fowler DM, Pritchard CC.

Genet Med. 2020 May;22(5):825-830. doi: 10.1038/s41436-019-0740-6. Epub 2020 Jan 8.

PubMed [citation]
PMID:
31911673
PMCID:
PMC7200594

Details of each submission

From Ambry Genetics, SCV001170550.5

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

Description

The p.V419G variant (also known as c.1256T>G), located in coding exon 9 of the BRCA1 gene, results from a T to G substitution at nucleotide position 1256. The valine at codon 419 is replaced by glycine, an amino acid with dissimilar properties. This amino acid position is not well conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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

From University of Washington Department of Laboratory Medicine, University of Washington, SCV003846067.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedcuration PubMed (1)

Description

Missense variant in a coldspot region where missense variants are very unlikely to be pathogenic (PMID:31911673).

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

Last Updated: May 7, 2024