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NM_007294.4(BRCA1):c.3037G>C (p.Glu1013Gln) AND Hereditary cancer-predisposing syndrome

Germline classification:
Conflicting interpretations of pathogenicity (2 submissions)
Last evaluated:
Feb 12, 2024
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:
RCV003157994.4

Allele description [Variation Report for NM_007294.4(BRCA1):c.3037G>C (p.Glu1013Gln)]

NM_007294.4(BRCA1):c.3037G>C (p.Glu1013Gln)

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.3037G>C (p.Glu1013Gln)
HGVS:
  • NC_000017.11:g.43092494C>G
  • NG_005905.2:g.125490G>C
  • NM_001407571.1:c.2824G>C
  • NM_001407581.1:c.3037G>C
  • NM_001407582.1:c.3037G>C
  • NM_001407583.1:c.3037G>C
  • NM_001407585.1:c.3037G>C
  • NM_001407587.1:c.3034G>C
  • NM_001407590.1:c.3034G>C
  • NM_001407591.1:c.3034G>C
  • NM_001407593.1:c.3037G>C
  • NM_001407594.1:c.3037G>C
  • NM_001407596.1:c.3037G>C
  • NM_001407597.1:c.3037G>C
  • NM_001407598.1:c.3037G>C
  • NM_001407602.1:c.3037G>C
  • NM_001407603.1:c.3037G>C
  • NM_001407605.1:c.3037G>C
  • NM_001407610.1:c.3034G>C
  • NM_001407611.1:c.3034G>C
  • NM_001407612.1:c.3034G>C
  • NM_001407613.1:c.3034G>C
  • NM_001407614.1:c.3034G>C
  • NM_001407615.1:c.3034G>C
  • NM_001407616.1:c.3037G>C
  • NM_001407617.1:c.3037G>C
  • NM_001407618.1:c.3037G>C
  • NM_001407619.1:c.3037G>C
  • NM_001407620.1:c.3037G>C
  • NM_001407621.1:c.3037G>C
  • NM_001407622.1:c.3037G>C
  • NM_001407623.1:c.3037G>C
  • NM_001407624.1:c.3037G>C
  • NM_001407625.1:c.3037G>C
  • NM_001407626.1:c.3037G>C
  • NM_001407627.1:c.3034G>C
  • NM_001407628.1:c.3034G>C
  • NM_001407629.1:c.3034G>C
  • NM_001407630.1:c.3034G>C
  • NM_001407631.1:c.3034G>C
  • NM_001407632.1:c.3034G>C
  • NM_001407633.1:c.3034G>C
  • NM_001407634.1:c.3034G>C
  • NM_001407635.1:c.3034G>C
  • NM_001407636.1:c.3034G>C
  • NM_001407637.1:c.3034G>C
  • NM_001407638.1:c.3034G>C
  • NM_001407639.1:c.3037G>C
  • NM_001407640.1:c.3037G>C
  • NM_001407641.1:c.3037G>C
  • NM_001407642.1:c.3037G>C
  • NM_001407644.1:c.3034G>C
  • NM_001407645.1:c.3034G>C
  • NM_001407646.1:c.3028G>C
  • NM_001407647.1:c.3028G>C
  • NM_001407648.1:c.2914G>C
  • NM_001407649.1:c.2911G>C
  • NM_001407652.1:c.3037G>C
  • NM_001407653.1:c.2959G>C
  • NM_001407654.1:c.2959G>C
  • NM_001407655.1:c.2959G>C
  • NM_001407656.1:c.2959G>C
  • NM_001407657.1:c.2959G>C
  • NM_001407658.1:c.2959G>C
  • NM_001407659.1:c.2956G>C
  • NM_001407660.1:c.2956G>C
  • NM_001407661.1:c.2956G>C
  • NM_001407662.1:c.2956G>C
  • NM_001407663.1:c.2959G>C
  • NM_001407664.1:c.2914G>C
  • NM_001407665.1:c.2914G>C
  • NM_001407666.1:c.2914G>C
  • NM_001407667.1:c.2914G>C
  • NM_001407668.1:c.2914G>C
  • NM_001407669.1:c.2914G>C
  • NM_001407670.1:c.2911G>C
  • NM_001407671.1:c.2911G>C
  • NM_001407672.1:c.2911G>C
  • NM_001407673.1:c.2911G>C
  • NM_001407674.1:c.2914G>C
  • NM_001407675.1:c.2914G>C
  • NM_001407676.1:c.2914G>C
  • NM_001407677.1:c.2914G>C
  • NM_001407678.1:c.2914G>C
  • NM_001407679.1:c.2914G>C
  • NM_001407680.1:c.2914G>C
  • NM_001407681.1:c.2914G>C
  • NM_001407682.1:c.2914G>C
  • NM_001407683.1:c.2914G>C
  • NM_001407684.1:c.3037G>C
  • NM_001407685.1:c.2911G>C
  • NM_001407686.1:c.2911G>C
  • NM_001407687.1:c.2911G>C
  • NM_001407688.1:c.2911G>C
  • NM_001407689.1:c.2911G>C
  • NM_001407690.1:c.2911G>C
  • NM_001407691.1:c.2911G>C
  • NM_001407692.1:c.2896G>C
  • NM_001407694.1:c.2896G>C
  • NM_001407695.1:c.2896G>C
  • NM_001407696.1:c.2896G>C
  • NM_001407697.1:c.2896G>C
  • NM_001407698.1:c.2896G>C
  • NM_001407724.1:c.2896G>C
  • NM_001407725.1:c.2896G>C
  • NM_001407726.1:c.2896G>C
  • NM_001407727.1:c.2896G>C
  • NM_001407728.1:c.2896G>C
  • NM_001407729.1:c.2896G>C
  • NM_001407730.1:c.2896G>C
  • NM_001407731.1:c.2896G>C
  • NM_001407732.1:c.2896G>C
  • NM_001407733.1:c.2896G>C
  • NM_001407734.1:c.2896G>C
  • NM_001407735.1:c.2896G>C
  • NM_001407736.1:c.2896G>C
  • NM_001407737.1:c.2896G>C
  • NM_001407738.1:c.2896G>C
  • NM_001407739.1:c.2896G>C
  • NM_001407740.1:c.2893G>C
  • NM_001407741.1:c.2893G>C
  • NM_001407742.1:c.2893G>C
  • NM_001407743.1:c.2893G>C
  • NM_001407744.1:c.2893G>C
  • NM_001407745.1:c.2893G>C
  • NM_001407746.1:c.2893G>C
  • NM_001407747.1:c.2893G>C
  • NM_001407748.1:c.2893G>C
  • NM_001407749.1:c.2893G>C
  • NM_001407750.1:c.2896G>C
  • NM_001407751.1:c.2896G>C
  • NM_001407752.1:c.2896G>C
  • NM_001407838.1:c.2893G>C
  • NM_001407839.1:c.2893G>C
  • NM_001407841.1:c.2893G>C
  • NM_001407842.1:c.2893G>C
  • NM_001407843.1:c.2893G>C
  • NM_001407844.1:c.2893G>C
  • NM_001407845.1:c.2893G>C
  • NM_001407846.1:c.2893G>C
  • NM_001407847.1:c.2893G>C
  • NM_001407848.1:c.2893G>C
  • NM_001407849.1:c.2893G>C
  • NM_001407850.1:c.2896G>C
  • NM_001407851.1:c.2896G>C
  • NM_001407852.1:c.2896G>C
  • NM_001407853.1:c.2824G>C
  • NM_001407854.1:c.3037G>C
  • NM_001407858.1:c.3037G>C
  • NM_001407859.1:c.3037G>C
  • NM_001407860.1:c.3034G>C
  • NM_001407861.1:c.3034G>C
  • NM_001407862.1:c.2836G>C
  • NM_001407863.1:c.2914G>C
  • NM_001407874.1:c.2833G>C
  • NM_001407875.1:c.2833G>C
  • NM_001407879.1:c.2827G>C
  • NM_001407881.1:c.2827G>C
  • NM_001407882.1:c.2827G>C
  • NM_001407884.1:c.2827G>C
  • NM_001407885.1:c.2827G>C
  • NM_001407886.1:c.2827G>C
  • NM_001407887.1:c.2827G>C
  • NM_001407889.1:c.2827G>C
  • NM_001407894.1:c.2824G>C
  • NM_001407895.1:c.2824G>C
  • NM_001407896.1:c.2824G>C
  • NM_001407897.1:c.2824G>C
  • NM_001407898.1:c.2824G>C
  • NM_001407899.1:c.2824G>C
  • NM_001407900.1:c.2827G>C
  • NM_001407902.1:c.2827G>C
  • NM_001407904.1:c.2827G>C
  • NM_001407906.1:c.2827G>C
  • NM_001407907.1:c.2827G>C
  • NM_001407908.1:c.2827G>C
  • NM_001407909.1:c.2827G>C
  • NM_001407910.1:c.2827G>C
  • NM_001407915.1:c.2824G>C
  • NM_001407916.1:c.2824G>C
  • NM_001407917.1:c.2824G>C
  • NM_001407918.1:c.2824G>C
  • NM_001407919.1:c.2914G>C
  • NM_001407920.1:c.2773G>C
  • NM_001407921.1:c.2773G>C
  • NM_001407922.1:c.2773G>C
  • NM_001407923.1:c.2773G>C
  • NM_001407924.1:c.2773G>C
  • NM_001407925.1:c.2773G>C
  • NM_001407926.1:c.2773G>C
  • NM_001407927.1:c.2773G>C
  • NM_001407928.1:c.2773G>C
  • NM_001407929.1:c.2773G>C
  • NM_001407930.1:c.2770G>C
  • NM_001407931.1:c.2770G>C
  • NM_001407932.1:c.2770G>C
  • NM_001407933.1:c.2773G>C
  • NM_001407934.1:c.2770G>C
  • NM_001407935.1:c.2773G>C
  • NM_001407936.1:c.2770G>C
  • NM_001407937.1:c.2914G>C
  • NM_001407938.1:c.2914G>C
  • NM_001407939.1:c.2914G>C
  • NM_001407940.1:c.2911G>C
  • NM_001407941.1:c.2911G>C
  • NM_001407942.1:c.2896G>C
  • NM_001407943.1:c.2893G>C
  • NM_001407944.1:c.2896G>C
  • NM_001407945.1:c.2896G>C
  • NM_001407946.1:c.2704G>C
  • NM_001407947.1:c.2704G>C
  • NM_001407948.1:c.2704G>C
  • NM_001407949.1:c.2704G>C
  • NM_001407950.1:c.2704G>C
  • NM_001407951.1:c.2704G>C
  • NM_001407952.1:c.2704G>C
  • NM_001407953.1:c.2704G>C
  • NM_001407954.1:c.2701G>C
  • NM_001407955.1:c.2701G>C
  • NM_001407956.1:c.2701G>C
  • NM_001407957.1:c.2704G>C
  • NM_001407958.1:c.2701G>C
  • NM_001407959.1:c.2656G>C
  • NM_001407960.1:c.2656G>C
  • NM_001407962.1:c.2653G>C
  • NM_001407963.1:c.2656G>C
  • NM_001407964.1:c.2893G>C
  • NM_001407965.1:c.2533G>C
  • NM_001407966.1:c.2149G>C
  • NM_001407967.1:c.2149G>C
  • NM_001407968.1:c.788-355G>C
  • NM_001407969.1:c.788-355G>C
  • NM_001407970.1:c.788-1462G>C
  • NM_001407971.1:c.788-1462G>C
  • NM_001407972.1:c.785-1462G>C
  • NM_001407973.1:c.788-1462G>C
  • NM_001407974.1:c.788-1462G>C
  • NM_001407975.1:c.788-1462G>C
  • NM_001407976.1:c.788-1462G>C
  • NM_001407977.1:c.788-1462G>C
  • NM_001407978.1:c.788-1462G>C
  • NM_001407979.1:c.788-1462G>C
  • NM_001407980.1:c.788-1462G>C
  • NM_001407981.1:c.788-1462G>C
  • NM_001407982.1:c.788-1462G>C
  • NM_001407983.1:c.788-1462G>C
  • NM_001407984.1:c.785-1462G>C
  • NM_001407985.1:c.785-1462G>C
  • NM_001407986.1:c.785-1462G>C
  • NM_001407990.1:c.788-1462G>C
  • NM_001407991.1:c.785-1462G>C
  • NM_001407992.1:c.785-1462G>C
  • NM_001407993.1:c.788-1462G>C
  • NM_001408392.1:c.785-1462G>C
  • NM_001408396.1:c.785-1462G>C
  • NM_001408397.1:c.785-1462G>C
  • NM_001408398.1:c.785-1462G>C
  • NM_001408399.1:c.785-1462G>C
  • NM_001408400.1:c.785-1462G>C
  • NM_001408401.1:c.785-1462G>C
  • NM_001408402.1:c.785-1462G>C
  • NM_001408403.1:c.788-1462G>C
  • NM_001408404.1:c.788-1462G>C
  • NM_001408406.1:c.791-1471G>C
  • NM_001408407.1:c.785-1462G>C
  • NM_001408408.1:c.779-1462G>C
  • NM_001408409.1:c.710-1462G>C
  • NM_001408410.1:c.647-1462G>C
  • NM_001408411.1:c.710-1462G>C
  • NM_001408412.1:c.710-1462G>C
  • NM_001408413.1:c.707-1462G>C
  • NM_001408414.1:c.710-1462G>C
  • NM_001408415.1:c.710-1462G>C
  • NM_001408416.1:c.707-1462G>C
  • NM_001408418.1:c.671-1462G>C
  • NM_001408419.1:c.671-1462G>C
  • NM_001408420.1:c.671-1462G>C
  • NM_001408421.1:c.668-1462G>C
  • NM_001408422.1:c.671-1462G>C
  • NM_001408423.1:c.671-1462G>C
  • NM_001408424.1:c.668-1462G>C
  • NM_001408425.1:c.665-1462G>C
  • NM_001408426.1:c.665-1462G>C
  • NM_001408427.1:c.665-1462G>C
  • NM_001408428.1:c.665-1462G>C
  • NM_001408429.1:c.665-1462G>C
  • NM_001408430.1:c.665-1462G>C
  • NM_001408431.1:c.668-1462G>C
  • NM_001408432.1:c.662-1462G>C
  • NM_001408433.1:c.662-1462G>C
  • NM_001408434.1:c.662-1462G>C
  • NM_001408435.1:c.662-1462G>C
  • NM_001408436.1:c.665-1462G>C
  • NM_001408437.1:c.665-1462G>C
  • NM_001408438.1:c.665-1462G>C
  • NM_001408439.1:c.665-1462G>C
  • NM_001408440.1:c.665-1462G>C
  • NM_001408441.1:c.665-1462G>C
  • NM_001408442.1:c.665-1462G>C
  • NM_001408443.1:c.665-1462G>C
  • NM_001408444.1:c.665-1462G>C
  • NM_001408445.1:c.662-1462G>C
  • NM_001408446.1:c.662-1462G>C
  • NM_001408447.1:c.662-1462G>C
  • NM_001408448.1:c.662-1462G>C
  • NM_001408450.1:c.662-1462G>C
  • NM_001408451.1:c.653-1462G>C
  • NM_001408452.1:c.647-1462G>C
  • NM_001408453.1:c.647-1462G>C
  • NM_001408454.1:c.647-1462G>C
  • NM_001408455.1:c.647-1462G>C
  • NM_001408456.1:c.647-1462G>C
  • NM_001408457.1:c.647-1462G>C
  • NM_001408458.1:c.647-1462G>C
  • NM_001408459.1:c.647-1462G>C
  • NM_001408460.1:c.647-1462G>C
  • NM_001408461.1:c.647-1462G>C
  • NM_001408462.1:c.644-1462G>C
  • NM_001408463.1:c.644-1462G>C
  • NM_001408464.1:c.644-1462G>C
  • NM_001408465.1:c.644-1462G>C
  • NM_001408466.1:c.647-1462G>C
  • NM_001408467.1:c.647-1462G>C
  • NM_001408468.1:c.644-1462G>C
  • NM_001408469.1:c.647-1462G>C
  • NM_001408470.1:c.644-1462G>C
  • NM_001408472.1:c.788-1462G>C
  • NM_001408473.1:c.785-1462G>C
  • NM_001408474.1:c.587-1462G>C
  • NM_001408475.1:c.584-1462G>C
  • NM_001408476.1:c.587-1462G>C
  • NM_001408478.1:c.578-1462G>C
  • NM_001408479.1:c.578-1462G>C
  • NM_001408480.1:c.578-1462G>C
  • NM_001408481.1:c.578-1462G>C
  • NM_001408482.1:c.578-1462G>C
  • NM_001408483.1:c.578-1462G>C
  • NM_001408484.1:c.578-1462G>C
  • NM_001408485.1:c.578-1462G>C
  • NM_001408489.1:c.578-1462G>C
  • NM_001408490.1:c.575-1462G>C
  • NM_001408491.1:c.575-1462G>C
  • NM_001408492.1:c.578-1462G>C
  • NM_001408493.1:c.575-1462G>C
  • NM_001408494.1:c.548-1462G>C
  • NM_001408495.1:c.545-1462G>C
  • NM_001408496.1:c.524-1462G>C
  • NM_001408497.1:c.524-1462G>C
  • NM_001408498.1:c.524-1462G>C
  • NM_001408499.1:c.524-1462G>C
  • NM_001408500.1:c.524-1462G>C
  • NM_001408501.1:c.524-1462G>C
  • NM_001408502.1:c.455-1462G>C
  • NM_001408503.1:c.521-1462G>C
  • NM_001408504.1:c.521-1462G>C
  • NM_001408505.1:c.521-1462G>C
  • NM_001408506.1:c.461-1462G>C
  • NM_001408507.1:c.461-1462G>C
  • NM_001408508.1:c.452-1462G>C
  • NM_001408509.1:c.452-1462G>C
  • NM_001408510.1:c.407-1462G>C
  • NM_001408511.1:c.404-1462G>C
  • NM_001408512.1:c.284-1462G>C
  • NM_001408513.1:c.578-1462G>C
  • NM_001408514.1:c.578-1462G>C
  • NM_007294.4:c.3037G>CMANE SELECT
  • NM_007297.4:c.2896G>C
  • NM_007298.4:c.788-1462G>C
  • NM_007299.4:c.788-1462G>C
  • NM_007300.4:c.3037G>C
  • NP_001394500.1:p.Glu942Gln
  • NP_001394510.1:p.Glu1013Gln
  • NP_001394511.1:p.Glu1013Gln
  • NP_001394512.1:p.Glu1013Gln
  • NP_001394514.1:p.Glu1013Gln
  • NP_001394516.1:p.Glu1012Gln
  • NP_001394519.1:p.Glu1012Gln
  • NP_001394520.1:p.Glu1012Gln
  • NP_001394522.1:p.Glu1013Gln
  • NP_001394523.1:p.Glu1013Gln
  • NP_001394525.1:p.Glu1013Gln
  • NP_001394526.1:p.Glu1013Gln
  • NP_001394527.1:p.Glu1013Gln
  • NP_001394531.1:p.Glu1013Gln
  • NP_001394532.1:p.Glu1013Gln
  • NP_001394534.1:p.Glu1013Gln
  • NP_001394539.1:p.Glu1012Gln
  • NP_001394540.1:p.Glu1012Gln
  • NP_001394541.1:p.Glu1012Gln
  • NP_001394542.1:p.Glu1012Gln
  • NP_001394543.1:p.Glu1012Gln
  • NP_001394544.1:p.Glu1012Gln
  • NP_001394545.1:p.Glu1013Gln
  • NP_001394546.1:p.Glu1013Gln
  • NP_001394547.1:p.Glu1013Gln
  • NP_001394548.1:p.Glu1013Gln
  • NP_001394549.1:p.Glu1013Gln
  • NP_001394550.1:p.Glu1013Gln
  • NP_001394551.1:p.Glu1013Gln
  • NP_001394552.1:p.Glu1013Gln
  • NP_001394553.1:p.Glu1013Gln
  • NP_001394554.1:p.Glu1013Gln
  • NP_001394555.1:p.Glu1013Gln
  • NP_001394556.1:p.Glu1012Gln
  • NP_001394557.1:p.Glu1012Gln
  • NP_001394558.1:p.Glu1012Gln
  • NP_001394559.1:p.Glu1012Gln
  • NP_001394560.1:p.Glu1012Gln
  • NP_001394561.1:p.Glu1012Gln
  • NP_001394562.1:p.Glu1012Gln
  • NP_001394563.1:p.Glu1012Gln
  • NP_001394564.1:p.Glu1012Gln
  • NP_001394565.1:p.Glu1012Gln
  • NP_001394566.1:p.Glu1012Gln
  • NP_001394567.1:p.Glu1012Gln
  • NP_001394568.1:p.Glu1013Gln
  • NP_001394569.1:p.Glu1013Gln
  • NP_001394570.1:p.Glu1013Gln
  • NP_001394571.1:p.Glu1013Gln
  • NP_001394573.1:p.Glu1012Gln
  • NP_001394574.1:p.Glu1012Gln
  • NP_001394575.1:p.Glu1010Gln
  • NP_001394576.1:p.Glu1010Gln
  • NP_001394577.1:p.Glu972Gln
  • NP_001394578.1:p.Glu971Gln
  • NP_001394581.1:p.Glu1013Gln
  • NP_001394582.1:p.Glu987Gln
  • NP_001394583.1:p.Glu987Gln
  • NP_001394584.1:p.Glu987Gln
  • NP_001394585.1:p.Glu987Gln
  • NP_001394586.1:p.Glu987Gln
  • NP_001394587.1:p.Glu987Gln
  • NP_001394588.1:p.Glu986Gln
  • NP_001394589.1:p.Glu986Gln
  • NP_001394590.1:p.Glu986Gln
  • NP_001394591.1:p.Glu986Gln
  • NP_001394592.1:p.Glu987Gln
  • NP_001394593.1:p.Glu972Gln
  • NP_001394594.1:p.Glu972Gln
  • NP_001394595.1:p.Glu972Gln
  • NP_001394596.1:p.Glu972Gln
  • NP_001394597.1:p.Glu972Gln
  • NP_001394598.1:p.Glu972Gln
  • NP_001394599.1:p.Glu971Gln
  • NP_001394600.1:p.Glu971Gln
  • NP_001394601.1:p.Glu971Gln
  • NP_001394602.1:p.Glu971Gln
  • NP_001394603.1:p.Glu972Gln
  • NP_001394604.1:p.Glu972Gln
  • NP_001394605.1:p.Glu972Gln
  • NP_001394606.1:p.Glu972Gln
  • NP_001394607.1:p.Glu972Gln
  • NP_001394608.1:p.Glu972Gln
  • NP_001394609.1:p.Glu972Gln
  • NP_001394610.1:p.Glu972Gln
  • NP_001394611.1:p.Glu972Gln
  • NP_001394612.1:p.Glu972Gln
  • NP_001394613.1:p.Glu1013Gln
  • NP_001394614.1:p.Glu971Gln
  • NP_001394615.1:p.Glu971Gln
  • NP_001394616.1:p.Glu971Gln
  • NP_001394617.1:p.Glu971Gln
  • NP_001394618.1:p.Glu971Gln
  • NP_001394619.1:p.Glu971Gln
  • NP_001394620.1:p.Glu971Gln
  • NP_001394621.1:p.Glu966Gln
  • NP_001394623.1:p.Glu966Gln
  • NP_001394624.1:p.Glu966Gln
  • NP_001394625.1:p.Glu966Gln
  • NP_001394626.1:p.Glu966Gln
  • NP_001394627.1:p.Glu966Gln
  • NP_001394653.1:p.Glu966Gln
  • NP_001394654.1:p.Glu966Gln
  • NP_001394655.1:p.Glu966Gln
  • NP_001394656.1:p.Glu966Gln
  • NP_001394657.1:p.Glu966Gln
  • NP_001394658.1:p.Glu966Gln
  • NP_001394659.1:p.Glu966Gln
  • NP_001394660.1:p.Glu966Gln
  • NP_001394661.1:p.Glu966Gln
  • NP_001394662.1:p.Glu966Gln
  • NP_001394663.1:p.Glu966Gln
  • NP_001394664.1:p.Glu966Gln
  • NP_001394665.1:p.Glu966Gln
  • NP_001394666.1:p.Glu966Gln
  • NP_001394667.1:p.Glu966Gln
  • NP_001394668.1:p.Glu966Gln
  • NP_001394669.1:p.Glu965Gln
  • NP_001394670.1:p.Glu965Gln
  • NP_001394671.1:p.Glu965Gln
  • NP_001394672.1:p.Glu965Gln
  • NP_001394673.1:p.Glu965Gln
  • NP_001394674.1:p.Glu965Gln
  • NP_001394675.1:p.Glu965Gln
  • NP_001394676.1:p.Glu965Gln
  • NP_001394677.1:p.Glu965Gln
  • NP_001394678.1:p.Glu965Gln
  • NP_001394679.1:p.Glu966Gln
  • NP_001394680.1:p.Glu966Gln
  • NP_001394681.1:p.Glu966Gln
  • NP_001394767.1:p.Glu965Gln
  • NP_001394768.1:p.Glu965Gln
  • NP_001394770.1:p.Glu965Gln
  • NP_001394771.1:p.Glu965Gln
  • NP_001394772.1:p.Glu965Gln
  • NP_001394773.1:p.Glu965Gln
  • NP_001394774.1:p.Glu965Gln
  • NP_001394775.1:p.Glu965Gln
  • NP_001394776.1:p.Glu965Gln
  • NP_001394777.1:p.Glu965Gln
  • NP_001394778.1:p.Glu965Gln
  • NP_001394779.1:p.Glu966Gln
  • NP_001394780.1:p.Glu966Gln
  • NP_001394781.1:p.Glu966Gln
  • NP_001394782.1:p.Glu942Gln
  • NP_001394783.1:p.Glu1013Gln
  • NP_001394787.1:p.Glu1013Gln
  • NP_001394788.1:p.Glu1013Gln
  • NP_001394789.1:p.Glu1012Gln
  • NP_001394790.1:p.Glu1012Gln
  • NP_001394791.1:p.Glu946Gln
  • NP_001394792.1:p.Glu972Gln
  • NP_001394803.1:p.Glu945Gln
  • NP_001394804.1:p.Glu945Gln
  • NP_001394808.1:p.Glu943Gln
  • NP_001394810.1:p.Glu943Gln
  • NP_001394811.1:p.Glu943Gln
  • NP_001394813.1:p.Glu943Gln
  • NP_001394814.1:p.Glu943Gln
  • NP_001394815.1:p.Glu943Gln
  • NP_001394816.1:p.Glu943Gln
  • NP_001394818.1:p.Glu943Gln
  • NP_001394823.1:p.Glu942Gln
  • NP_001394824.1:p.Glu942Gln
  • NP_001394825.1:p.Glu942Gln
  • NP_001394826.1:p.Glu942Gln
  • NP_001394827.1:p.Glu942Gln
  • NP_001394828.1:p.Glu942Gln
  • NP_001394829.1:p.Glu943Gln
  • NP_001394831.1:p.Glu943Gln
  • NP_001394833.1:p.Glu943Gln
  • NP_001394835.1:p.Glu943Gln
  • NP_001394836.1:p.Glu943Gln
  • NP_001394837.1:p.Glu943Gln
  • NP_001394838.1:p.Glu943Gln
  • NP_001394839.1:p.Glu943Gln
  • NP_001394844.1:p.Glu942Gln
  • NP_001394845.1:p.Glu942Gln
  • NP_001394846.1:p.Glu942Gln
  • NP_001394847.1:p.Glu942Gln
  • NP_001394848.1:p.Glu972Gln
  • NP_001394849.1:p.Glu925Gln
  • NP_001394850.1:p.Glu925Gln
  • NP_001394851.1:p.Glu925Gln
  • NP_001394852.1:p.Glu925Gln
  • NP_001394853.1:p.Glu925Gln
  • NP_001394854.1:p.Glu925Gln
  • NP_001394855.1:p.Glu925Gln
  • NP_001394856.1:p.Glu925Gln
  • NP_001394857.1:p.Glu925Gln
  • NP_001394858.1:p.Glu925Gln
  • NP_001394859.1:p.Glu924Gln
  • NP_001394860.1:p.Glu924Gln
  • NP_001394861.1:p.Glu924Gln
  • NP_001394862.1:p.Glu925Gln
  • NP_001394863.1:p.Glu924Gln
  • NP_001394864.1:p.Glu925Gln
  • NP_001394865.1:p.Glu924Gln
  • NP_001394866.1:p.Glu972Gln
  • NP_001394867.1:p.Glu972Gln
  • NP_001394868.1:p.Glu972Gln
  • NP_001394869.1:p.Glu971Gln
  • NP_001394870.1:p.Glu971Gln
  • NP_001394871.1:p.Glu966Gln
  • NP_001394872.1:p.Glu965Gln
  • NP_001394873.1:p.Glu966Gln
  • NP_001394874.1:p.Glu966Gln
  • NP_001394875.1:p.Glu902Gln
  • NP_001394876.1:p.Glu902Gln
  • NP_001394877.1:p.Glu902Gln
  • NP_001394878.1:p.Glu902Gln
  • NP_001394879.1:p.Glu902Gln
  • NP_001394880.1:p.Glu902Gln
  • NP_001394881.1:p.Glu902Gln
  • NP_001394882.1:p.Glu902Gln
  • NP_001394883.1:p.Glu901Gln
  • NP_001394884.1:p.Glu901Gln
  • NP_001394885.1:p.Glu901Gln
  • NP_001394886.1:p.Glu902Gln
  • NP_001394887.1:p.Glu901Gln
  • NP_001394888.1:p.Glu886Gln
  • NP_001394889.1:p.Glu886Gln
  • NP_001394891.1:p.Glu885Gln
  • NP_001394892.1:p.Glu886Gln
  • NP_001394893.1:p.Glu965Gln
  • NP_001394894.1:p.Glu845Gln
  • NP_001394895.1:p.Glu717Gln
  • NP_001394896.1:p.Glu717Gln
  • NP_009225.1:p.Glu1013Gln
  • NP_009225.1:p.Glu1013Gln
  • NP_009228.2:p.Glu966Gln
  • NP_009231.2:p.Glu1013Gln
  • LRG_292t1:c.3037G>C
  • LRG_292:g.125490G>C
  • LRG_292p1:p.Glu1013Gln
  • NC_000017.10:g.41244511C>G
  • NM_007294.3:c.3037G>C
  • NR_027676.1:n.3173G>C
Protein change:
E1010Q
Molecular consequence:
  • NM_001407968.1:c.788-355G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.788-355G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.791-1471G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.779-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.710-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.710-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.710-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.707-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.710-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.710-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.707-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.671-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.671-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.671-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.668-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.671-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.671-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.668-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.668-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.662-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.662-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.662-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.662-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.665-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.662-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.662-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.662-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.662-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.662-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.653-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.644-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.644-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.644-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.644-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.644-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.647-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.644-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.785-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.587-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.584-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.587-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.575-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.575-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.575-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.548-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.545-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.524-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.524-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.524-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.524-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.524-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.524-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.455-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.521-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.521-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.521-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.461-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.461-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.452-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.452-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.407-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.404-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.284-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.578-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.788-1462G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.3028G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.3028G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.2959G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.2959G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.2959G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.2959G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.2959G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.2959G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.2956G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.2956G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.2956G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.2956G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.2959G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.3034G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.2836G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.2833G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.2833G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.2827G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.2824G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.2770G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.2770G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.2770G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.2770G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.2773G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.2770G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.2914G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.2911G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.2704G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.2704G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.2704G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.2704G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.2704G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.2704G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.2704G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.2704G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.2701G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.2701G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.2701G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.2704G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.2701G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.2656G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.2656G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.2653G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.2656G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.2893G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.2533G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.2149G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.2149G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.3037G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.2896G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.3037G>C - 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

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003849172University 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]

SCV005026031Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Feb 12, 2024) 		germlineclinical testing

Citation Link

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 University of Washington Department of Laboratory Medicine, University of Washington, SCV003849172.1

#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

From Ambry Genetics, SCV005026031.1

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

Description

The p.E1013Q variant (also known as c.3037G>C), located in coding exon 9 of the BRCA1 gene, results from a G to C substitution at nucleotide position 3037. The glutamic acid at codon 1013 is replaced by glutamine, an amino acid with highly similar properties. This amino acid position is poorly conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Based on the available evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: May 7, 2024