NM_007294.4(BRCA1):c.3031G>T (p.Glu1011Ter) AND Hereditary breast ovarian cancer syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Mar 9, 2021
- Review status:
- 1 star out of maximum of 4 starscriteria provided, single submitter
- Somatic classification
of clinical impact: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Somatic classification
of oncogenicity: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Record status:
- current
- Accession:
- RCV001994555.5
Allele description [Variation Report for NM_007294.4(BRCA1):c.3031G>T (p.Glu1011Ter)]
NM_007294.4(BRCA1):c.3031G>T (p.Glu1011Ter)
- 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.3031G>T (p.Glu1011Ter)
- HGVS:
- NC_000017.11:g.43092500C>A
- NG_005905.2:g.125484G>T
- NM_001407571.1:c.2818G>T
- NM_001407581.1:c.3031G>T
- NM_001407582.1:c.3031G>T
- NM_001407583.1:c.3031G>T
- NM_001407585.1:c.3031G>T
- NM_001407587.1:c.3028G>T
- NM_001407590.1:c.3028G>T
- NM_001407591.1:c.3028G>T
- NM_001407593.1:c.3031G>T
- NM_001407594.1:c.3031G>T
- NM_001407596.1:c.3031G>T
- NM_001407597.1:c.3031G>T
- NM_001407598.1:c.3031G>T
- NM_001407602.1:c.3031G>T
- NM_001407603.1:c.3031G>T
- NM_001407605.1:c.3031G>T
- NM_001407610.1:c.3028G>T
- NM_001407611.1:c.3028G>T
- NM_001407612.1:c.3028G>T
- NM_001407613.1:c.3028G>T
- NM_001407614.1:c.3028G>T
- NM_001407615.1:c.3028G>T
- NM_001407616.1:c.3031G>T
- NM_001407617.1:c.3031G>T
- NM_001407618.1:c.3031G>T
- NM_001407619.1:c.3031G>T
- NM_001407620.1:c.3031G>T
- NM_001407621.1:c.3031G>T
- NM_001407622.1:c.3031G>T
- NM_001407623.1:c.3031G>T
- NM_001407624.1:c.3031G>T
- NM_001407625.1:c.3031G>T
- NM_001407626.1:c.3031G>T
- NM_001407627.1:c.3028G>T
- NM_001407628.1:c.3028G>T
- NM_001407629.1:c.3028G>T
- NM_001407630.1:c.3028G>T
- NM_001407631.1:c.3028G>T
- NM_001407632.1:c.3028G>T
- NM_001407633.1:c.3028G>T
- NM_001407634.1:c.3028G>T
- NM_001407635.1:c.3028G>T
- NM_001407636.1:c.3028G>T
- NM_001407637.1:c.3028G>T
- NM_001407638.1:c.3028G>T
- NM_001407639.1:c.3031G>T
- NM_001407640.1:c.3031G>T
- NM_001407641.1:c.3031G>T
- NM_001407642.1:c.3031G>T
- NM_001407644.1:c.3028G>T
- NM_001407645.1:c.3028G>T
- NM_001407646.1:c.3022G>T
- NM_001407647.1:c.3022G>T
- NM_001407648.1:c.2908G>T
- NM_001407649.1:c.2905G>T
- NM_001407652.1:c.3031G>T
- NM_001407653.1:c.2953G>T
- NM_001407654.1:c.2953G>T
- NM_001407655.1:c.2953G>T
- NM_001407656.1:c.2953G>T
- NM_001407657.1:c.2953G>T
- NM_001407658.1:c.2953G>T
- NM_001407659.1:c.2950G>T
- NM_001407660.1:c.2950G>T
- NM_001407661.1:c.2950G>T
- NM_001407662.1:c.2950G>T
- NM_001407663.1:c.2953G>T
- NM_001407664.1:c.2908G>T
- NM_001407665.1:c.2908G>T
- NM_001407666.1:c.2908G>T
- NM_001407667.1:c.2908G>T
- NM_001407668.1:c.2908G>T
- NM_001407669.1:c.2908G>T
- NM_001407670.1:c.2905G>T
- NM_001407671.1:c.2905G>T
- NM_001407672.1:c.2905G>T
- NM_001407673.1:c.2905G>T
- NM_001407674.1:c.2908G>T
- NM_001407675.1:c.2908G>T
- NM_001407676.1:c.2908G>T
- NM_001407677.1:c.2908G>T
- NM_001407678.1:c.2908G>T
- NM_001407679.1:c.2908G>T
- NM_001407680.1:c.2908G>T
- NM_001407681.1:c.2908G>T
- NM_001407682.1:c.2908G>T
- NM_001407683.1:c.2908G>T
- NM_001407684.1:c.3031G>T
- NM_001407685.1:c.2905G>T
- NM_001407686.1:c.2905G>T
- NM_001407687.1:c.2905G>T
- NM_001407688.1:c.2905G>T
- NM_001407689.1:c.2905G>T
- NM_001407690.1:c.2905G>T
- NM_001407691.1:c.2905G>T
- NM_001407692.1:c.2890G>T
- NM_001407694.1:c.2890G>T
- NM_001407695.1:c.2890G>T
- NM_001407696.1:c.2890G>T
- NM_001407697.1:c.2890G>T
- NM_001407698.1:c.2890G>T
- NM_001407724.1:c.2890G>T
- NM_001407725.1:c.2890G>T
- NM_001407726.1:c.2890G>T
- NM_001407727.1:c.2890G>T
- NM_001407728.1:c.2890G>T
- NM_001407729.1:c.2890G>T
- NM_001407730.1:c.2890G>T
- NM_001407731.1:c.2890G>T
- NM_001407732.1:c.2890G>T
- NM_001407733.1:c.2890G>T
- NM_001407734.1:c.2890G>T
- NM_001407735.1:c.2890G>T
- NM_001407736.1:c.2890G>T
- NM_001407737.1:c.2890G>T
- NM_001407738.1:c.2890G>T
- NM_001407739.1:c.2890G>T
- NM_001407740.1:c.2887G>T
- NM_001407741.1:c.2887G>T
- NM_001407742.1:c.2887G>T
- NM_001407743.1:c.2887G>T
- NM_001407744.1:c.2887G>T
- NM_001407745.1:c.2887G>T
- NM_001407746.1:c.2887G>T
- NM_001407747.1:c.2887G>T
- NM_001407748.1:c.2887G>T
- NM_001407749.1:c.2887G>T
- NM_001407750.1:c.2890G>T
- NM_001407751.1:c.2890G>T
- NM_001407752.1:c.2890G>T
- NM_001407838.1:c.2887G>T
- NM_001407839.1:c.2887G>T
- NM_001407841.1:c.2887G>T
- NM_001407842.1:c.2887G>T
- NM_001407843.1:c.2887G>T
- NM_001407844.1:c.2887G>T
- NM_001407845.1:c.2887G>T
- NM_001407846.1:c.2887G>T
- NM_001407847.1:c.2887G>T
- NM_001407848.1:c.2887G>T
- NM_001407849.1:c.2887G>T
- NM_001407850.1:c.2890G>T
- NM_001407851.1:c.2890G>T
- NM_001407852.1:c.2890G>T
- NM_001407853.1:c.2818G>T
- NM_001407854.1:c.3031G>T
- NM_001407858.1:c.3031G>T
- NM_001407859.1:c.3031G>T
- NM_001407860.1:c.3028G>T
- NM_001407861.1:c.3028G>T
- NM_001407862.1:c.2830G>T
- NM_001407863.1:c.2908G>T
- NM_001407874.1:c.2827G>T
- NM_001407875.1:c.2827G>T
- NM_001407879.1:c.2821G>T
- NM_001407881.1:c.2821G>T
- NM_001407882.1:c.2821G>T
- NM_001407884.1:c.2821G>T
- NM_001407885.1:c.2821G>T
- NM_001407886.1:c.2821G>T
- NM_001407887.1:c.2821G>T
- NM_001407889.1:c.2821G>T
- NM_001407894.1:c.2818G>T
- NM_001407895.1:c.2818G>T
- NM_001407896.1:c.2818G>T
- NM_001407897.1:c.2818G>T
- NM_001407898.1:c.2818G>T
- NM_001407899.1:c.2818G>T
- NM_001407900.1:c.2821G>T
- NM_001407902.1:c.2821G>T
- NM_001407904.1:c.2821G>T
- NM_001407906.1:c.2821G>T
- NM_001407907.1:c.2821G>T
- NM_001407908.1:c.2821G>T
- NM_001407909.1:c.2821G>T
- NM_001407910.1:c.2821G>T
- NM_001407915.1:c.2818G>T
- NM_001407916.1:c.2818G>T
- NM_001407917.1:c.2818G>T
- NM_001407918.1:c.2818G>T
- NM_001407919.1:c.2908G>T
- NM_001407920.1:c.2767G>T
- NM_001407921.1:c.2767G>T
- NM_001407922.1:c.2767G>T
- NM_001407923.1:c.2767G>T
- NM_001407924.1:c.2767G>T
- NM_001407925.1:c.2767G>T
- NM_001407926.1:c.2767G>T
- NM_001407927.1:c.2767G>T
- NM_001407928.1:c.2767G>T
- NM_001407929.1:c.2767G>T
- NM_001407930.1:c.2764G>T
- NM_001407931.1:c.2764G>T
- NM_001407932.1:c.2764G>T
- NM_001407933.1:c.2767G>T
- NM_001407934.1:c.2764G>T
- NM_001407935.1:c.2767G>T
- NM_001407936.1:c.2764G>T
- NM_001407937.1:c.2908G>T
- NM_001407938.1:c.2908G>T
- NM_001407939.1:c.2908G>T
- NM_001407940.1:c.2905G>T
- NM_001407941.1:c.2905G>T
- NM_001407942.1:c.2890G>T
- NM_001407943.1:c.2887G>T
- NM_001407944.1:c.2890G>T
- NM_001407945.1:c.2890G>T
- NM_001407946.1:c.2698G>T
- NM_001407947.1:c.2698G>T
- NM_001407948.1:c.2698G>T
- NM_001407949.1:c.2698G>T
- NM_001407950.1:c.2698G>T
- NM_001407951.1:c.2698G>T
- NM_001407952.1:c.2698G>T
- NM_001407953.1:c.2698G>T
- NM_001407954.1:c.2695G>T
- NM_001407955.1:c.2695G>T
- NM_001407956.1:c.2695G>T
- NM_001407957.1:c.2698G>T
- NM_001407958.1:c.2695G>T
- NM_001407959.1:c.2650G>T
- NM_001407960.1:c.2650G>T
- NM_001407962.1:c.2647G>T
- NM_001407963.1:c.2650G>T
- NM_001407964.1:c.2887G>T
- NM_001407965.1:c.2527G>T
- NM_001407966.1:c.2143G>T
- NM_001407967.1:c.2143G>T
- NM_001407968.1:c.788-361G>T
- NM_001407969.1:c.788-361G>T
- NM_001407970.1:c.788-1468G>T
- NM_001407971.1:c.788-1468G>T
- NM_001407972.1:c.785-1468G>T
- NM_001407973.1:c.788-1468G>T
- NM_001407974.1:c.788-1468G>T
- NM_001407975.1:c.788-1468G>T
- NM_001407976.1:c.788-1468G>T
- NM_001407977.1:c.788-1468G>T
- NM_001407978.1:c.788-1468G>T
- NM_001407979.1:c.788-1468G>T
- NM_001407980.1:c.788-1468G>T
- NM_001407981.1:c.788-1468G>T
- NM_001407982.1:c.788-1468G>T
- NM_001407983.1:c.788-1468G>T
- NM_001407984.1:c.785-1468G>T
- NM_001407985.1:c.785-1468G>T
- NM_001407986.1:c.785-1468G>T
- NM_001407990.1:c.788-1468G>T
- NM_001407991.1:c.785-1468G>T
- NM_001407992.1:c.785-1468G>T
- NM_001407993.1:c.788-1468G>T
- NM_001408392.1:c.785-1468G>T
- NM_001408396.1:c.785-1468G>T
- NM_001408397.1:c.785-1468G>T
- NM_001408398.1:c.785-1468G>T
- NM_001408399.1:c.785-1468G>T
- NM_001408400.1:c.785-1468G>T
- NM_001408401.1:c.785-1468G>T
- NM_001408402.1:c.785-1468G>T
- NM_001408403.1:c.788-1468G>T
- NM_001408404.1:c.788-1468G>T
- NM_001408406.1:c.791-1477G>T
- NM_001408407.1:c.785-1468G>T
- NM_001408408.1:c.779-1468G>T
- NM_001408409.1:c.710-1468G>T
- NM_001408410.1:c.647-1468G>T
- NM_001408411.1:c.710-1468G>T
- NM_001408412.1:c.710-1468G>T
- NM_001408413.1:c.707-1468G>T
- NM_001408414.1:c.710-1468G>T
- NM_001408415.1:c.710-1468G>T
- NM_001408416.1:c.707-1468G>T
- NM_001408418.1:c.671-1468G>T
- NM_001408419.1:c.671-1468G>T
- NM_001408420.1:c.671-1468G>T
- NM_001408421.1:c.668-1468G>T
- NM_001408422.1:c.671-1468G>T
- NM_001408423.1:c.671-1468G>T
- NM_001408424.1:c.668-1468G>T
- NM_001408425.1:c.665-1468G>T
- NM_001408426.1:c.665-1468G>T
- NM_001408427.1:c.665-1468G>T
- NM_001408428.1:c.665-1468G>T
- NM_001408429.1:c.665-1468G>T
- NM_001408430.1:c.665-1468G>T
- NM_001408431.1:c.668-1468G>T
- NM_001408432.1:c.662-1468G>T
- NM_001408433.1:c.662-1468G>T
- NM_001408434.1:c.662-1468G>T
- NM_001408435.1:c.662-1468G>T
- NM_001408436.1:c.665-1468G>T
- NM_001408437.1:c.665-1468G>T
- NM_001408438.1:c.665-1468G>T
- NM_001408439.1:c.665-1468G>T
- NM_001408440.1:c.665-1468G>T
- NM_001408441.1:c.665-1468G>T
- NM_001408442.1:c.665-1468G>T
- NM_001408443.1:c.665-1468G>T
- NM_001408444.1:c.665-1468G>T
- NM_001408445.1:c.662-1468G>T
- NM_001408446.1:c.662-1468G>T
- NM_001408447.1:c.662-1468G>T
- NM_001408448.1:c.662-1468G>T
- NM_001408450.1:c.662-1468G>T
- NM_001408451.1:c.653-1468G>T
- NM_001408452.1:c.647-1468G>T
- NM_001408453.1:c.647-1468G>T
- NM_001408454.1:c.647-1468G>T
- NM_001408455.1:c.647-1468G>T
- NM_001408456.1:c.647-1468G>T
- NM_001408457.1:c.647-1468G>T
- NM_001408458.1:c.647-1468G>T
- NM_001408459.1:c.647-1468G>T
- NM_001408460.1:c.647-1468G>T
- NM_001408461.1:c.647-1468G>T
- NM_001408462.1:c.644-1468G>T
- NM_001408463.1:c.644-1468G>T
- NM_001408464.1:c.644-1468G>T
- NM_001408465.1:c.644-1468G>T
- NM_001408466.1:c.647-1468G>T
- NM_001408467.1:c.647-1468G>T
- NM_001408468.1:c.644-1468G>T
- NM_001408469.1:c.647-1468G>T
- NM_001408470.1:c.644-1468G>T
- NM_001408472.1:c.788-1468G>T
- NM_001408473.1:c.785-1468G>T
- NM_001408474.1:c.587-1468G>T
- NM_001408475.1:c.584-1468G>T
- NM_001408476.1:c.587-1468G>T
- NM_001408478.1:c.578-1468G>T
- NM_001408479.1:c.578-1468G>T
- NM_001408480.1:c.578-1468G>T
- NM_001408481.1:c.578-1468G>T
- NM_001408482.1:c.578-1468G>T
- NM_001408483.1:c.578-1468G>T
- NM_001408484.1:c.578-1468G>T
- NM_001408485.1:c.578-1468G>T
- NM_001408489.1:c.578-1468G>T
- NM_001408490.1:c.575-1468G>T
- NM_001408491.1:c.575-1468G>T
- NM_001408492.1:c.578-1468G>T
- NM_001408493.1:c.575-1468G>T
- NM_001408494.1:c.548-1468G>T
- NM_001408495.1:c.545-1468G>T
- NM_001408496.1:c.524-1468G>T
- NM_001408497.1:c.524-1468G>T
- NM_001408498.1:c.524-1468G>T
- NM_001408499.1:c.524-1468G>T
- NM_001408500.1:c.524-1468G>T
- NM_001408501.1:c.524-1468G>T
- NM_001408502.1:c.455-1468G>T
- NM_001408503.1:c.521-1468G>T
- NM_001408504.1:c.521-1468G>T
- NM_001408505.1:c.521-1468G>T
- NM_001408506.1:c.461-1468G>T
- NM_001408507.1:c.461-1468G>T
- NM_001408508.1:c.452-1468G>T
- NM_001408509.1:c.452-1468G>T
- NM_001408510.1:c.407-1468G>T
- NM_001408511.1:c.404-1468G>T
- NM_001408512.1:c.284-1468G>T
- NM_001408513.1:c.578-1468G>T
- NM_001408514.1:c.578-1468G>T
- NM_007294.4:c.3031G>TMANE SELECT
- NM_007297.4:c.2890G>T
- NM_007298.4:c.788-1468G>T
- NM_007299.4:c.788-1468G>T
- NM_007300.4:c.3031G>T
- NP_001394500.1:p.Glu940Ter
- NP_001394510.1:p.Glu1011Ter
- NP_001394511.1:p.Glu1011Ter
- NP_001394512.1:p.Glu1011Ter
- NP_001394514.1:p.Glu1011Ter
- NP_001394516.1:p.Glu1010Ter
- NP_001394519.1:p.Glu1010Ter
- NP_001394520.1:p.Glu1010Ter
- NP_001394522.1:p.Glu1011Ter
- NP_001394523.1:p.Glu1011Ter
- NP_001394525.1:p.Glu1011Ter
- NP_001394526.1:p.Glu1011Ter
- NP_001394527.1:p.Glu1011Ter
- NP_001394531.1:p.Glu1011Ter
- NP_001394532.1:p.Glu1011Ter
- NP_001394534.1:p.Glu1011Ter
- NP_001394539.1:p.Glu1010Ter
- NP_001394540.1:p.Glu1010Ter
- NP_001394541.1:p.Glu1010Ter
- NP_001394542.1:p.Glu1010Ter
- NP_001394543.1:p.Glu1010Ter
- NP_001394544.1:p.Glu1010Ter
- NP_001394545.1:p.Glu1011Ter
- NP_001394546.1:p.Glu1011Ter
- NP_001394547.1:p.Glu1011Ter
- NP_001394548.1:p.Glu1011Ter
- NP_001394549.1:p.Glu1011Ter
- NP_001394550.1:p.Glu1011Ter
- NP_001394551.1:p.Glu1011Ter
- NP_001394552.1:p.Glu1011Ter
- NP_001394553.1:p.Glu1011Ter
- NP_001394554.1:p.Glu1011Ter
- NP_001394555.1:p.Glu1011Ter
- NP_001394556.1:p.Glu1010Ter
- NP_001394557.1:p.Glu1010Ter
- NP_001394558.1:p.Glu1010Ter
- NP_001394559.1:p.Glu1010Ter
- NP_001394560.1:p.Glu1010Ter
- NP_001394561.1:p.Glu1010Ter
- NP_001394562.1:p.Glu1010Ter
- NP_001394563.1:p.Glu1010Ter
- NP_001394564.1:p.Glu1010Ter
- NP_001394565.1:p.Glu1010Ter
- NP_001394566.1:p.Glu1010Ter
- NP_001394567.1:p.Glu1010Ter
- NP_001394568.1:p.Glu1011Ter
- NP_001394569.1:p.Glu1011Ter
- NP_001394570.1:p.Glu1011Ter
- NP_001394571.1:p.Glu1011Ter
- NP_001394573.1:p.Glu1010Ter
- NP_001394574.1:p.Glu1010Ter
- NP_001394575.1:p.Glu1008Ter
- NP_001394576.1:p.Glu1008Ter
- NP_001394577.1:p.Glu970Ter
- NP_001394578.1:p.Glu969Ter
- NP_001394581.1:p.Glu1011Ter
- NP_001394582.1:p.Glu985Ter
- NP_001394583.1:p.Glu985Ter
- NP_001394584.1:p.Glu985Ter
- NP_001394585.1:p.Glu985Ter
- NP_001394586.1:p.Glu985Ter
- NP_001394587.1:p.Glu985Ter
- NP_001394588.1:p.Glu984Ter
- NP_001394589.1:p.Glu984Ter
- NP_001394590.1:p.Glu984Ter
- NP_001394591.1:p.Glu984Ter
- NP_001394592.1:p.Glu985Ter
- NP_001394593.1:p.Glu970Ter
- NP_001394594.1:p.Glu970Ter
- NP_001394595.1:p.Glu970Ter
- NP_001394596.1:p.Glu970Ter
- NP_001394597.1:p.Glu970Ter
- NP_001394598.1:p.Glu970Ter
- NP_001394599.1:p.Glu969Ter
- NP_001394600.1:p.Glu969Ter
- NP_001394601.1:p.Glu969Ter
- NP_001394602.1:p.Glu969Ter
- NP_001394603.1:p.Glu970Ter
- NP_001394604.1:p.Glu970Ter
- NP_001394605.1:p.Glu970Ter
- NP_001394606.1:p.Glu970Ter
- NP_001394607.1:p.Glu970Ter
- NP_001394608.1:p.Glu970Ter
- NP_001394609.1:p.Glu970Ter
- NP_001394610.1:p.Glu970Ter
- NP_001394611.1:p.Glu970Ter
- NP_001394612.1:p.Glu970Ter
- NP_001394613.1:p.Glu1011Ter
- NP_001394614.1:p.Glu969Ter
- NP_001394615.1:p.Glu969Ter
- NP_001394616.1:p.Glu969Ter
- NP_001394617.1:p.Glu969Ter
- NP_001394618.1:p.Glu969Ter
- NP_001394619.1:p.Glu969Ter
- NP_001394620.1:p.Glu969Ter
- NP_001394621.1:p.Glu964Ter
- NP_001394623.1:p.Glu964Ter
- NP_001394624.1:p.Glu964Ter
- NP_001394625.1:p.Glu964Ter
- NP_001394626.1:p.Glu964Ter
- NP_001394627.1:p.Glu964Ter
- NP_001394653.1:p.Glu964Ter
- NP_001394654.1:p.Glu964Ter
- NP_001394655.1:p.Glu964Ter
- NP_001394656.1:p.Glu964Ter
- NP_001394657.1:p.Glu964Ter
- NP_001394658.1:p.Glu964Ter
- NP_001394659.1:p.Glu964Ter
- NP_001394660.1:p.Glu964Ter
- NP_001394661.1:p.Glu964Ter
- NP_001394662.1:p.Glu964Ter
- NP_001394663.1:p.Glu964Ter
- NP_001394664.1:p.Glu964Ter
- NP_001394665.1:p.Glu964Ter
- NP_001394666.1:p.Glu964Ter
- NP_001394667.1:p.Glu964Ter
- NP_001394668.1:p.Glu964Ter
- NP_001394669.1:p.Glu963Ter
- NP_001394670.1:p.Glu963Ter
- NP_001394671.1:p.Glu963Ter
- NP_001394672.1:p.Glu963Ter
- NP_001394673.1:p.Glu963Ter
- NP_001394674.1:p.Glu963Ter
- NP_001394675.1:p.Glu963Ter
- NP_001394676.1:p.Glu963Ter
- NP_001394677.1:p.Glu963Ter
- NP_001394678.1:p.Glu963Ter
- NP_001394679.1:p.Glu964Ter
- NP_001394680.1:p.Glu964Ter
- NP_001394681.1:p.Glu964Ter
- NP_001394767.1:p.Glu963Ter
- NP_001394768.1:p.Glu963Ter
- NP_001394770.1:p.Glu963Ter
- NP_001394771.1:p.Glu963Ter
- NP_001394772.1:p.Glu963Ter
- NP_001394773.1:p.Glu963Ter
- NP_001394774.1:p.Glu963Ter
- NP_001394775.1:p.Glu963Ter
- NP_001394776.1:p.Glu963Ter
- NP_001394777.1:p.Glu963Ter
- NP_001394778.1:p.Glu963Ter
- NP_001394779.1:p.Glu964Ter
- NP_001394780.1:p.Glu964Ter
- NP_001394781.1:p.Glu964Ter
- NP_001394782.1:p.Glu940Ter
- NP_001394783.1:p.Glu1011Ter
- NP_001394787.1:p.Glu1011Ter
- NP_001394788.1:p.Glu1011Ter
- NP_001394789.1:p.Glu1010Ter
- NP_001394790.1:p.Glu1010Ter
- NP_001394791.1:p.Glu944Ter
- NP_001394792.1:p.Glu970Ter
- NP_001394803.1:p.Glu943Ter
- NP_001394804.1:p.Glu943Ter
- NP_001394808.1:p.Glu941Ter
- NP_001394810.1:p.Glu941Ter
- NP_001394811.1:p.Glu941Ter
- NP_001394813.1:p.Glu941Ter
- NP_001394814.1:p.Glu941Ter
- NP_001394815.1:p.Glu941Ter
- NP_001394816.1:p.Glu941Ter
- NP_001394818.1:p.Glu941Ter
- NP_001394823.1:p.Glu940Ter
- NP_001394824.1:p.Glu940Ter
- NP_001394825.1:p.Glu940Ter
- NP_001394826.1:p.Glu940Ter
- NP_001394827.1:p.Glu940Ter
- NP_001394828.1:p.Glu940Ter
- NP_001394829.1:p.Glu941Ter
- NP_001394831.1:p.Glu941Ter
- NP_001394833.1:p.Glu941Ter
- NP_001394835.1:p.Glu941Ter
- NP_001394836.1:p.Glu941Ter
- NP_001394837.1:p.Glu941Ter
- NP_001394838.1:p.Glu941Ter
- NP_001394839.1:p.Glu941Ter
- NP_001394844.1:p.Glu940Ter
- NP_001394845.1:p.Glu940Ter
- NP_001394846.1:p.Glu940Ter
- NP_001394847.1:p.Glu940Ter
- NP_001394848.1:p.Glu970Ter
- NP_001394849.1:p.Glu923Ter
- NP_001394850.1:p.Glu923Ter
- NP_001394851.1:p.Glu923Ter
- NP_001394852.1:p.Glu923Ter
- NP_001394853.1:p.Glu923Ter
- NP_001394854.1:p.Glu923Ter
- NP_001394855.1:p.Glu923Ter
- NP_001394856.1:p.Glu923Ter
- NP_001394857.1:p.Glu923Ter
- NP_001394858.1:p.Glu923Ter
- NP_001394859.1:p.Glu922Ter
- NP_001394860.1:p.Glu922Ter
- NP_001394861.1:p.Glu922Ter
- NP_001394862.1:p.Glu923Ter
- NP_001394863.1:p.Glu922Ter
- NP_001394864.1:p.Glu923Ter
- NP_001394865.1:p.Glu922Ter
- NP_001394866.1:p.Glu970Ter
- NP_001394867.1:p.Glu970Ter
- NP_001394868.1:p.Glu970Ter
- NP_001394869.1:p.Glu969Ter
- NP_001394870.1:p.Glu969Ter
- NP_001394871.1:p.Glu964Ter
- NP_001394872.1:p.Glu963Ter
- NP_001394873.1:p.Glu964Ter
- NP_001394874.1:p.Glu964Ter
- NP_001394875.1:p.Glu900Ter
- NP_001394876.1:p.Glu900Ter
- NP_001394877.1:p.Glu900Ter
- NP_001394878.1:p.Glu900Ter
- NP_001394879.1:p.Glu900Ter
- NP_001394880.1:p.Glu900Ter
- NP_001394881.1:p.Glu900Ter
- NP_001394882.1:p.Glu900Ter
- NP_001394883.1:p.Glu899Ter
- NP_001394884.1:p.Glu899Ter
- NP_001394885.1:p.Glu899Ter
- NP_001394886.1:p.Glu900Ter
- NP_001394887.1:p.Glu899Ter
- NP_001394888.1:p.Glu884Ter
- NP_001394889.1:p.Glu884Ter
- NP_001394891.1:p.Glu883Ter
- NP_001394892.1:p.Glu884Ter
- NP_001394893.1:p.Glu963Ter
- NP_001394894.1:p.Glu843Ter
- NP_001394895.1:p.Glu715Ter
- NP_001394896.1:p.Glu715Ter
- NP_009225.1:p.Glu1011Ter
- NP_009225.1:p.Glu1011Ter
- NP_009228.2:p.Glu964Ter
- NP_009231.2:p.Glu1011Ter
- LRG_292t1:c.3031G>T
- LRG_292:g.125484G>T
- LRG_292p1:p.Glu1011Ter
- NC_000017.10:g.41244517C>A
- NM_007294.3:c.3031G>T
- NR_027676.1:n.3167G>T
This HGVS expression did not pass validation- Protein change:
- E1008*
- Links:
- dbSNP: rs876659974
- NCBI 1000 Genomes Browser:
- rs876659974
- Molecular consequence:
- NM_001407968.1:c.788-361G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407969.1:c.788-361G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407970.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407971.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407972.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407973.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407974.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407975.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407976.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407977.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407978.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407979.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407980.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407981.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407982.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407983.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407984.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407985.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407986.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407990.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407991.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407992.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407993.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408392.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408396.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408397.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408398.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408399.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408400.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408401.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408402.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408403.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408404.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408406.1:c.791-1477G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408407.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408408.1:c.779-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408409.1:c.710-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408410.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408411.1:c.710-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408412.1:c.710-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408413.1:c.707-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408414.1:c.710-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408415.1:c.710-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408416.1:c.707-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408418.1:c.671-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408419.1:c.671-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408420.1:c.671-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408421.1:c.668-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408422.1:c.671-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408423.1:c.671-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408424.1:c.668-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408425.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408426.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408427.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408428.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408429.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408430.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408431.1:c.668-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408432.1:c.662-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408433.1:c.662-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408434.1:c.662-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408435.1:c.662-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408436.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408437.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408438.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408439.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408440.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408441.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408442.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408443.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408444.1:c.665-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408445.1:c.662-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408446.1:c.662-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408447.1:c.662-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408448.1:c.662-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408450.1:c.662-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408451.1:c.653-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408452.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408453.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408454.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408455.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408456.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408457.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408458.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408459.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408460.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408461.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408462.1:c.644-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408463.1:c.644-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408464.1:c.644-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408465.1:c.644-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408466.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408467.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408468.1:c.644-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408469.1:c.647-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408470.1:c.644-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408472.1:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408473.1:c.785-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408474.1:c.587-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408475.1:c.584-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408476.1:c.587-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408478.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408479.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408480.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408481.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408482.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408483.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408484.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408485.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408489.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408490.1:c.575-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408491.1:c.575-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408492.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408493.1:c.575-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408494.1:c.548-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408495.1:c.545-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408496.1:c.524-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408497.1:c.524-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408498.1:c.524-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408499.1:c.524-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408500.1:c.524-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408501.1:c.524-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408502.1:c.455-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408503.1:c.521-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408504.1:c.521-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408505.1:c.521-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408506.1:c.461-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408507.1:c.461-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408508.1:c.452-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408509.1:c.452-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408510.1:c.407-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408511.1:c.404-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408512.1:c.284-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408513.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408514.1:c.578-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_007298.4:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_007299.4:c.788-1468G>T - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407571.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407581.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407582.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407583.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407585.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407587.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407590.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407591.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407593.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407594.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407596.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407597.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407598.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407602.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407603.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407605.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407610.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407611.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407612.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407613.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407614.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407615.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407616.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407617.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407618.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407619.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407620.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407621.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407622.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407623.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407624.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407625.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407626.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407627.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407628.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407629.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407630.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407631.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407632.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407633.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407634.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407635.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407636.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407637.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407638.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407639.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407640.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407641.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407642.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407644.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407645.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407646.1:c.3022G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407647.1:c.3022G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407648.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407649.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407652.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407653.1:c.2953G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407654.1:c.2953G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407655.1:c.2953G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407656.1:c.2953G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407657.1:c.2953G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407658.1:c.2953G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407659.1:c.2950G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407660.1:c.2950G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407661.1:c.2950G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407662.1:c.2950G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407663.1:c.2953G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407664.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407665.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407666.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407667.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407668.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407669.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407670.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407671.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407672.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407673.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407674.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407675.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407676.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407677.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407678.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407679.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407680.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407681.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407682.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407683.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407684.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407685.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407686.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407687.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407688.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407689.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407690.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407691.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407692.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407694.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407695.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407696.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407697.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407698.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407724.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407725.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407726.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407727.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407728.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407729.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407730.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407731.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407732.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407733.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407734.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407735.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407736.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407737.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407738.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407739.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407740.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407741.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407742.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407743.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407744.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407745.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407746.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407747.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407748.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407749.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407750.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407751.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407752.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407838.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407839.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407841.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407842.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407843.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407844.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407845.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407846.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407847.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407848.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407849.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407850.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407851.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407852.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407853.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407854.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407858.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407859.1:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407860.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407861.1:c.3028G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407862.1:c.2830G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407863.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407874.1:c.2827G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407875.1:c.2827G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407879.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407881.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407882.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407884.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407885.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407886.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407887.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407889.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407894.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407895.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407896.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407897.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407898.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407899.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407900.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407902.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407904.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407906.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407907.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407908.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407909.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407910.1:c.2821G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407915.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407916.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407917.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407918.1:c.2818G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407919.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407920.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407921.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407922.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407923.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407924.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407925.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407926.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407927.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407928.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407929.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407930.1:c.2764G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407931.1:c.2764G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407932.1:c.2764G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407933.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407934.1:c.2764G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407935.1:c.2767G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407936.1:c.2764G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407937.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407938.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407939.1:c.2908G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407940.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407941.1:c.2905G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407942.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407943.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407944.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407945.1:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407946.1:c.2698G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407947.1:c.2698G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407948.1:c.2698G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407949.1:c.2698G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407950.1:c.2698G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407951.1:c.2698G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407952.1:c.2698G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407953.1:c.2698G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407954.1:c.2695G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407955.1:c.2695G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407956.1:c.2695G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407957.1:c.2698G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407958.1:c.2695G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407959.1:c.2650G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407960.1:c.2650G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407962.1:c.2647G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407963.1:c.2650G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407964.1:c.2887G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407965.1:c.2527G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407966.1:c.2143G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_001407967.1:c.2143G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_007294.4:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_007297.4:c.2890G>T - nonsense - [Sequence Ontology: SO:0001587]
- NM_007300.4:c.3031G>T - nonsense - [Sequence Ontology: SO:0001587]
Condition(s)
- Name:
- Hereditary breast ovarian cancer syndrome
- Synonyms:
- Hereditary breast and ovarian cancer syndrome; Hereditary breast and ovarian cancer; Hereditary breast and ovarian cancer syndrome (HBOC); See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0003582; MeSH: D061325; MedGen: C0677776; Orphanet: 145
Assertion and evidence details
Submission Accession | Submitter | Review Status (Assertion method) | Clinical Significance (Last evaluated) | Origin | Method | Citations |
---|---|---|---|---|---|---|
SCV002233068 | Labcorp Genetics (formerly Invitae), Labcorp | criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) | Pathogenic (Mar 9, 2021) | germline | clinical testing |
Summary from all submissions
Ethnicity | Origin | Affected | Individuals | Families | Chromosomes tested | Number Tested | Family history | Method |
---|---|---|---|---|---|---|---|---|
not provided | germline | unknown | not provided | not provided | not provided | not provided | not provided | clinical testing |
Citations
PubMed
Borg A, Haile RW, Malone KE, Capanu M, Diep A, Törngren T, Teraoka S, Begg CB, Thomas DC, Concannon P, Mellemkjaer L, Bernstein L, Tellhed L, Xue S, Olson ER, Liang X, Dolle J, Børresen-Dale AL, Bernstein JL.
Hum Mutat. 2010 Mar;31(3):E1200-40. doi: 10.1002/humu.21202.
- PMID:
- 20104584
- PMCID:
- PMC2928257
Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.
Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.
Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.
- PMID:
- 28492532
- PMCID:
- PMC5632818
Details of each submission
From Labcorp Genetics (formerly Invitae), Labcorp, SCV002233068.3
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | PubMed (2) |
Description
For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals with BRCA1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Glu1011*) in the BRCA1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in BRCA1 are known to be pathogenic (PMID: 20104584).
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | unknown | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
Last Updated: Sep 29, 2024