U.S. flag

An official website of the United States government

NM_007294.4(BRCA1):c.1971A>G (p.Gln657=) AND Malignant tumor of breast

Germline classification:
Benign (1 submission)
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
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:
RCV001353799.9

Allele description [Variation Report for NM_007294.4(BRCA1):c.1971A>G (p.Gln657=)]

NM_007294.4(BRCA1):c.1971A>G (p.Gln657=)

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.1971A>G (p.Gln657=)
Other names:
2090A/G; p.Q657Q:CAA>CAG; 2090 A>G; NP_009225.1:p.Gln657=
HGVS:
  • NC_000017.11:g.43093560T>C
  • NG_005905.2:g.124424A>G
  • NM_001407571.1:c.1758A>G
  • NM_001407581.1:c.1971A>G
  • NM_001407582.1:c.1971A>G
  • NM_001407583.1:c.1971A>G
  • NM_001407585.1:c.1971A>G
  • NM_001407587.1:c.1968A>G
  • NM_001407590.1:c.1968A>G
  • NM_001407591.1:c.1968A>G
  • NM_001407593.1:c.1971A>G
  • NM_001407594.1:c.1971A>G
  • NM_001407596.1:c.1971A>G
  • NM_001407597.1:c.1971A>G
  • NM_001407598.1:c.1971A>G
  • NM_001407602.1:c.1971A>G
  • NM_001407603.1:c.1971A>G
  • NM_001407605.1:c.1971A>G
  • NM_001407610.1:c.1968A>G
  • NM_001407611.1:c.1968A>G
  • NM_001407612.1:c.1968A>G
  • NM_001407613.1:c.1968A>G
  • NM_001407614.1:c.1968A>G
  • NM_001407615.1:c.1968A>G
  • NM_001407616.1:c.1971A>G
  • NM_001407617.1:c.1971A>G
  • NM_001407618.1:c.1971A>G
  • NM_001407619.1:c.1971A>G
  • NM_001407620.1:c.1971A>G
  • NM_001407621.1:c.1971A>G
  • NM_001407622.1:c.1971A>G
  • NM_001407623.1:c.1971A>G
  • NM_001407624.1:c.1971A>G
  • NM_001407625.1:c.1971A>G
  • NM_001407626.1:c.1971A>G
  • NM_001407627.1:c.1968A>G
  • NM_001407628.1:c.1968A>G
  • NM_001407629.1:c.1968A>G
  • NM_001407630.1:c.1968A>G
  • NM_001407631.1:c.1968A>G
  • NM_001407632.1:c.1968A>G
  • NM_001407633.1:c.1968A>G
  • NM_001407634.1:c.1968A>G
  • NM_001407635.1:c.1968A>G
  • NM_001407636.1:c.1968A>G
  • NM_001407637.1:c.1968A>G
  • NM_001407638.1:c.1968A>G
  • NM_001407639.1:c.1971A>G
  • NM_001407640.1:c.1971A>G
  • NM_001407641.1:c.1971A>G
  • NM_001407642.1:c.1971A>G
  • NM_001407644.1:c.1968A>G
  • NM_001407645.1:c.1968A>G
  • NM_001407646.1:c.1962A>G
  • NM_001407647.1:c.1962A>G
  • NM_001407648.1:c.1848A>G
  • NM_001407649.1:c.1845A>G
  • NM_001407652.1:c.1971A>G
  • NM_001407653.1:c.1893A>G
  • NM_001407654.1:c.1893A>G
  • NM_001407655.1:c.1893A>G
  • NM_001407656.1:c.1893A>G
  • NM_001407657.1:c.1893A>G
  • NM_001407658.1:c.1893A>G
  • NM_001407659.1:c.1890A>G
  • NM_001407660.1:c.1890A>G
  • NM_001407661.1:c.1890A>G
  • NM_001407662.1:c.1890A>G
  • NM_001407663.1:c.1893A>G
  • NM_001407664.1:c.1848A>G
  • NM_001407665.1:c.1848A>G
  • NM_001407666.1:c.1848A>G
  • NM_001407667.1:c.1848A>G
  • NM_001407668.1:c.1848A>G
  • NM_001407669.1:c.1848A>G
  • NM_001407670.1:c.1845A>G
  • NM_001407671.1:c.1845A>G
  • NM_001407672.1:c.1845A>G
  • NM_001407673.1:c.1845A>G
  • NM_001407674.1:c.1848A>G
  • NM_001407675.1:c.1848A>G
  • NM_001407676.1:c.1848A>G
  • NM_001407677.1:c.1848A>G
  • NM_001407678.1:c.1848A>G
  • NM_001407679.1:c.1848A>G
  • NM_001407680.1:c.1848A>G
  • NM_001407681.1:c.1848A>G
  • NM_001407682.1:c.1848A>G
  • NM_001407683.1:c.1848A>G
  • NM_001407684.1:c.1971A>G
  • NM_001407685.1:c.1845A>G
  • NM_001407686.1:c.1845A>G
  • NM_001407687.1:c.1845A>G
  • NM_001407688.1:c.1845A>G
  • NM_001407689.1:c.1845A>G
  • NM_001407690.1:c.1845A>G
  • NM_001407691.1:c.1845A>G
  • NM_001407692.1:c.1830A>G
  • NM_001407694.1:c.1830A>G
  • NM_001407695.1:c.1830A>G
  • NM_001407696.1:c.1830A>G
  • NM_001407697.1:c.1830A>G
  • NM_001407698.1:c.1830A>G
  • NM_001407724.1:c.1830A>G
  • NM_001407725.1:c.1830A>G
  • NM_001407726.1:c.1830A>G
  • NM_001407727.1:c.1830A>G
  • NM_001407728.1:c.1830A>G
  • NM_001407729.1:c.1830A>G
  • NM_001407730.1:c.1830A>G
  • NM_001407731.1:c.1830A>G
  • NM_001407732.1:c.1830A>G
  • NM_001407733.1:c.1830A>G
  • NM_001407734.1:c.1830A>G
  • NM_001407735.1:c.1830A>G
  • NM_001407736.1:c.1830A>G
  • NM_001407737.1:c.1830A>G
  • NM_001407738.1:c.1830A>G
  • NM_001407739.1:c.1830A>G
  • NM_001407740.1:c.1827A>G
  • NM_001407741.1:c.1827A>G
  • NM_001407742.1:c.1827A>G
  • NM_001407743.1:c.1827A>G
  • NM_001407744.1:c.1827A>G
  • NM_001407745.1:c.1827A>G
  • NM_001407746.1:c.1827A>G
  • NM_001407747.1:c.1827A>G
  • NM_001407748.1:c.1827A>G
  • NM_001407749.1:c.1827A>G
  • NM_001407750.1:c.1830A>G
  • NM_001407751.1:c.1830A>G
  • NM_001407752.1:c.1830A>G
  • NM_001407838.1:c.1827A>G
  • NM_001407839.1:c.1827A>G
  • NM_001407841.1:c.1827A>G
  • NM_001407842.1:c.1827A>G
  • NM_001407843.1:c.1827A>G
  • NM_001407844.1:c.1827A>G
  • NM_001407845.1:c.1827A>G
  • NM_001407846.1:c.1827A>G
  • NM_001407847.1:c.1827A>G
  • NM_001407848.1:c.1827A>G
  • NM_001407849.1:c.1827A>G
  • NM_001407850.1:c.1830A>G
  • NM_001407851.1:c.1830A>G
  • NM_001407852.1:c.1830A>G
  • NM_001407853.1:c.1758A>G
  • NM_001407854.1:c.1971A>G
  • NM_001407858.1:c.1971A>G
  • NM_001407859.1:c.1971A>G
  • NM_001407860.1:c.1968A>G
  • NM_001407861.1:c.1968A>G
  • NM_001407862.1:c.1770A>G
  • NM_001407863.1:c.1848A>G
  • NM_001407874.1:c.1767A>G
  • NM_001407875.1:c.1767A>G
  • NM_001407879.1:c.1761A>G
  • NM_001407881.1:c.1761A>G
  • NM_001407882.1:c.1761A>G
  • NM_001407884.1:c.1761A>G
  • NM_001407885.1:c.1761A>G
  • NM_001407886.1:c.1761A>G
  • NM_001407887.1:c.1761A>G
  • NM_001407889.1:c.1761A>G
  • NM_001407894.1:c.1758A>G
  • NM_001407895.1:c.1758A>G
  • NM_001407896.1:c.1758A>G
  • NM_001407897.1:c.1758A>G
  • NM_001407898.1:c.1758A>G
  • NM_001407899.1:c.1758A>G
  • NM_001407900.1:c.1761A>G
  • NM_001407902.1:c.1761A>G
  • NM_001407904.1:c.1761A>G
  • NM_001407906.1:c.1761A>G
  • NM_001407907.1:c.1761A>G
  • NM_001407908.1:c.1761A>G
  • NM_001407909.1:c.1761A>G
  • NM_001407910.1:c.1761A>G
  • NM_001407915.1:c.1758A>G
  • NM_001407916.1:c.1758A>G
  • NM_001407917.1:c.1758A>G
  • NM_001407918.1:c.1758A>G
  • NM_001407919.1:c.1848A>G
  • NM_001407920.1:c.1707A>G
  • NM_001407921.1:c.1707A>G
  • NM_001407922.1:c.1707A>G
  • NM_001407923.1:c.1707A>G
  • NM_001407924.1:c.1707A>G
  • NM_001407925.1:c.1707A>G
  • NM_001407926.1:c.1707A>G
  • NM_001407927.1:c.1707A>G
  • NM_001407928.1:c.1707A>G
  • NM_001407929.1:c.1707A>G
  • NM_001407930.1:c.1704A>G
  • NM_001407931.1:c.1704A>G
  • NM_001407932.1:c.1704A>G
  • NM_001407933.1:c.1707A>G
  • NM_001407934.1:c.1704A>G
  • NM_001407935.1:c.1707A>G
  • NM_001407936.1:c.1704A>G
  • NM_001407937.1:c.1848A>G
  • NM_001407938.1:c.1848A>G
  • NM_001407939.1:c.1848A>G
  • NM_001407940.1:c.1845A>G
  • NM_001407941.1:c.1845A>G
  • NM_001407942.1:c.1830A>G
  • NM_001407943.1:c.1827A>G
  • NM_001407944.1:c.1830A>G
  • NM_001407945.1:c.1830A>G
  • NM_001407946.1:c.1638A>G
  • NM_001407947.1:c.1638A>G
  • NM_001407948.1:c.1638A>G
  • NM_001407949.1:c.1638A>G
  • NM_001407950.1:c.1638A>G
  • NM_001407951.1:c.1638A>G
  • NM_001407952.1:c.1638A>G
  • NM_001407953.1:c.1638A>G
  • NM_001407954.1:c.1635A>G
  • NM_001407955.1:c.1635A>G
  • NM_001407956.1:c.1635A>G
  • NM_001407957.1:c.1638A>G
  • NM_001407958.1:c.1635A>G
  • NM_001407959.1:c.1590A>G
  • NM_001407960.1:c.1590A>G
  • NM_001407962.1:c.1587A>G
  • NM_001407963.1:c.1590A>G
  • NM_001407964.1:c.1827A>G
  • NM_001407965.1:c.1467A>G
  • NM_001407966.1:c.1083A>G
  • NM_001407967.1:c.1083A>G
  • NM_001407968.1:c.787+1184A>G
  • NM_001407969.1:c.787+1184A>G
  • NM_001407970.1:c.787+1184A>G
  • NM_001407971.1:c.787+1184A>G
  • NM_001407972.1:c.784+1184A>G
  • NM_001407973.1:c.787+1184A>G
  • NM_001407974.1:c.787+1184A>G
  • NM_001407975.1:c.787+1184A>G
  • NM_001407976.1:c.787+1184A>G
  • NM_001407977.1:c.787+1184A>G
  • NM_001407978.1:c.787+1184A>G
  • NM_001407979.1:c.787+1184A>G
  • NM_001407980.1:c.787+1184A>G
  • NM_001407981.1:c.787+1184A>G
  • NM_001407982.1:c.787+1184A>G
  • NM_001407983.1:c.787+1184A>G
  • NM_001407984.1:c.784+1184A>G
  • NM_001407985.1:c.784+1184A>G
  • NM_001407986.1:c.784+1184A>G
  • NM_001407990.1:c.787+1184A>G
  • NM_001407991.1:c.784+1184A>G
  • NM_001407992.1:c.784+1184A>G
  • NM_001407993.1:c.787+1184A>G
  • NM_001408392.1:c.784+1184A>G
  • NM_001408396.1:c.784+1184A>G
  • NM_001408397.1:c.784+1184A>G
  • NM_001408398.1:c.784+1184A>G
  • NM_001408399.1:c.784+1184A>G
  • NM_001408400.1:c.784+1184A>G
  • NM_001408401.1:c.784+1184A>G
  • NM_001408402.1:c.784+1184A>G
  • NM_001408403.1:c.787+1184A>G
  • NM_001408404.1:c.787+1184A>G
  • NM_001408406.1:c.790+1181A>G
  • NM_001408407.1:c.784+1184A>G
  • NM_001408408.1:c.778+1184A>G
  • NM_001408409.1:c.709+1184A>G
  • NM_001408410.1:c.646+1184A>G
  • NM_001408411.1:c.709+1184A>G
  • NM_001408412.1:c.709+1184A>G
  • NM_001408413.1:c.706+1184A>G
  • NM_001408414.1:c.709+1184A>G
  • NM_001408415.1:c.709+1184A>G
  • NM_001408416.1:c.706+1184A>G
  • NM_001408418.1:c.670+2286A>G
  • NM_001408419.1:c.670+2286A>G
  • NM_001408420.1:c.670+2286A>G
  • NM_001408421.1:c.667+2286A>G
  • NM_001408422.1:c.670+2286A>G
  • NM_001408423.1:c.670+2286A>G
  • NM_001408424.1:c.667+2286A>G
  • NM_001408425.1:c.664+1184A>G
  • NM_001408426.1:c.664+1184A>G
  • NM_001408427.1:c.664+1184A>G
  • NM_001408428.1:c.664+1184A>G
  • NM_001408429.1:c.664+1184A>G
  • NM_001408430.1:c.664+1184A>G
  • NM_001408431.1:c.667+2286A>G
  • NM_001408432.1:c.661+1184A>G
  • NM_001408433.1:c.661+1184A>G
  • NM_001408434.1:c.661+1184A>G
  • NM_001408435.1:c.661+1184A>G
  • NM_001408436.1:c.664+1184A>G
  • NM_001408437.1:c.664+1184A>G
  • NM_001408438.1:c.664+1184A>G
  • NM_001408439.1:c.664+1184A>G
  • NM_001408440.1:c.664+1184A>G
  • NM_001408441.1:c.664+1184A>G
  • NM_001408442.1:c.664+1184A>G
  • NM_001408443.1:c.664+1184A>G
  • NM_001408444.1:c.664+1184A>G
  • NM_001408445.1:c.661+1184A>G
  • NM_001408446.1:c.661+1184A>G
  • NM_001408447.1:c.661+1184A>G
  • NM_001408448.1:c.661+1184A>G
  • NM_001408450.1:c.661+1184A>G
  • NM_001408451.1:c.652+1184A>G
  • NM_001408452.1:c.646+1184A>G
  • NM_001408453.1:c.646+1184A>G
  • NM_001408454.1:c.646+1184A>G
  • NM_001408455.1:c.646+1184A>G
  • NM_001408456.1:c.646+1184A>G
  • NM_001408457.1:c.646+1184A>G
  • NM_001408458.1:c.646+1184A>G
  • NM_001408459.1:c.646+1184A>G
  • NM_001408460.1:c.646+1184A>G
  • NM_001408461.1:c.646+1184A>G
  • NM_001408462.1:c.643+1184A>G
  • NM_001408463.1:c.643+1184A>G
  • NM_001408464.1:c.643+1184A>G
  • NM_001408465.1:c.643+1184A>G
  • NM_001408466.1:c.646+1184A>G
  • NM_001408467.1:c.646+1184A>G
  • NM_001408468.1:c.643+1184A>G
  • NM_001408469.1:c.646+1184A>G
  • NM_001408470.1:c.643+1184A>G
  • NM_001408472.1:c.787+1184A>G
  • NM_001408473.1:c.784+1184A>G
  • NM_001408474.1:c.586+1184A>G
  • NM_001408475.1:c.583+1184A>G
  • NM_001408476.1:c.586+1184A>G
  • NM_001408478.1:c.577+1184A>G
  • NM_001408479.1:c.577+1184A>G
  • NM_001408480.1:c.577+1184A>G
  • NM_001408481.1:c.577+1184A>G
  • NM_001408482.1:c.577+1184A>G
  • NM_001408483.1:c.577+1184A>G
  • NM_001408484.1:c.577+1184A>G
  • NM_001408485.1:c.577+1184A>G
  • NM_001408489.1:c.577+1184A>G
  • NM_001408490.1:c.574+1184A>G
  • NM_001408491.1:c.574+1184A>G
  • NM_001408492.1:c.577+1184A>G
  • NM_001408493.1:c.574+1184A>G
  • NM_001408494.1:c.548-2528A>G
  • NM_001408495.1:c.545-2528A>G
  • NM_001408496.1:c.523+1184A>G
  • NM_001408497.1:c.523+1184A>G
  • NM_001408498.1:c.523+1184A>G
  • NM_001408499.1:c.523+1184A>G
  • NM_001408500.1:c.523+1184A>G
  • NM_001408501.1:c.523+1184A>G
  • NM_001408502.1:c.454+1184A>G
  • NM_001408503.1:c.520+1184A>G
  • NM_001408504.1:c.520+1184A>G
  • NM_001408505.1:c.520+1184A>G
  • NM_001408506.1:c.460+2286A>G
  • NM_001408507.1:c.460+2286A>G
  • NM_001408508.1:c.451+1184A>G
  • NM_001408509.1:c.451+1184A>G
  • NM_001408510.1:c.406+1184A>G
  • NM_001408511.1:c.404-2528A>G
  • NM_001408512.1:c.283+1184A>G
  • NM_001408513.1:c.577+1184A>G
  • NM_001408514.1:c.577+1184A>G
  • NM_007294.4:c.1971A>GMANE SELECT
  • NM_007297.4:c.1830A>G
  • NM_007298.4:c.787+1184A>G
  • NM_007299.4:c.787+1184A>G
  • NM_007300.4:c.1971A>G
  • NP_001394500.1:p.Gln586=
  • NP_001394510.1:p.Gln657=
  • NP_001394511.1:p.Gln657=
  • NP_001394512.1:p.Gln657=
  • NP_001394514.1:p.Gln657=
  • NP_001394516.1:p.Gln656=
  • NP_001394519.1:p.Gln656=
  • NP_001394520.1:p.Gln656=
  • NP_001394522.1:p.Gln657=
  • NP_001394523.1:p.Gln657=
  • NP_001394525.1:p.Gln657=
  • NP_001394526.1:p.Gln657=
  • NP_001394527.1:p.Gln657=
  • NP_001394531.1:p.Gln657=
  • NP_001394532.1:p.Gln657=
  • NP_001394534.1:p.Gln657=
  • NP_001394539.1:p.Gln656=
  • NP_001394540.1:p.Gln656=
  • NP_001394541.1:p.Gln656=
  • NP_001394542.1:p.Gln656=
  • NP_001394543.1:p.Gln656=
  • NP_001394544.1:p.Gln656=
  • NP_001394545.1:p.Gln657=
  • NP_001394546.1:p.Gln657=
  • NP_001394547.1:p.Gln657=
  • NP_001394548.1:p.Gln657=
  • NP_001394549.1:p.Gln657=
  • NP_001394550.1:p.Gln657=
  • NP_001394551.1:p.Gln657=
  • NP_001394552.1:p.Gln657=
  • NP_001394553.1:p.Gln657=
  • NP_001394554.1:p.Gln657=
  • NP_001394555.1:p.Gln657=
  • NP_001394556.1:p.Gln656=
  • NP_001394557.1:p.Gln656=
  • NP_001394558.1:p.Gln656=
  • NP_001394559.1:p.Gln656=
  • NP_001394560.1:p.Gln656=
  • NP_001394561.1:p.Gln656=
  • NP_001394562.1:p.Gln656=
  • NP_001394563.1:p.Gln656=
  • NP_001394564.1:p.Gln656=
  • NP_001394565.1:p.Gln656=
  • NP_001394566.1:p.Gln656=
  • NP_001394567.1:p.Gln656=
  • NP_001394568.1:p.Gln657=
  • NP_001394569.1:p.Gln657=
  • NP_001394570.1:p.Gln657=
  • NP_001394571.1:p.Gln657=
  • NP_001394573.1:p.Gln656=
  • NP_001394574.1:p.Gln656=
  • NP_001394575.1:p.Gln654=
  • NP_001394576.1:p.Gln654=
  • NP_001394577.1:p.Gln616=
  • NP_001394578.1:p.Gln615=
  • NP_001394581.1:p.Gln657=
  • NP_001394582.1:p.Gln631=
  • NP_001394583.1:p.Gln631=
  • NP_001394584.1:p.Gln631=
  • NP_001394585.1:p.Gln631=
  • NP_001394586.1:p.Gln631=
  • NP_001394587.1:p.Gln631=
  • NP_001394588.1:p.Gln630=
  • NP_001394589.1:p.Gln630=
  • NP_001394590.1:p.Gln630=
  • NP_001394591.1:p.Gln630=
  • NP_001394592.1:p.Gln631=
  • NP_001394593.1:p.Gln616=
  • NP_001394594.1:p.Gln616=
  • NP_001394595.1:p.Gln616=
  • NP_001394596.1:p.Gln616=
  • NP_001394597.1:p.Gln616=
  • NP_001394598.1:p.Gln616=
  • NP_001394599.1:p.Gln615=
  • NP_001394600.1:p.Gln615=
  • NP_001394601.1:p.Gln615=
  • NP_001394602.1:p.Gln615=
  • NP_001394603.1:p.Gln616=
  • NP_001394604.1:p.Gln616=
  • NP_001394605.1:p.Gln616=
  • NP_001394606.1:p.Gln616=
  • NP_001394607.1:p.Gln616=
  • NP_001394608.1:p.Gln616=
  • NP_001394609.1:p.Gln616=
  • NP_001394610.1:p.Gln616=
  • NP_001394611.1:p.Gln616=
  • NP_001394612.1:p.Gln616=
  • NP_001394613.1:p.Gln657=
  • NP_001394614.1:p.Gln615=
  • NP_001394615.1:p.Gln615=
  • NP_001394616.1:p.Gln615=
  • NP_001394617.1:p.Gln615=
  • NP_001394618.1:p.Gln615=
  • NP_001394619.1:p.Gln615=
  • NP_001394620.1:p.Gln615=
  • NP_001394621.1:p.Gln610=
  • NP_001394623.1:p.Gln610=
  • NP_001394624.1:p.Gln610=
  • NP_001394625.1:p.Gln610=
  • NP_001394626.1:p.Gln610=
  • NP_001394627.1:p.Gln610=
  • NP_001394653.1:p.Gln610=
  • NP_001394654.1:p.Gln610=
  • NP_001394655.1:p.Gln610=
  • NP_001394656.1:p.Gln610=
  • NP_001394657.1:p.Gln610=
  • NP_001394658.1:p.Gln610=
  • NP_001394659.1:p.Gln610=
  • NP_001394660.1:p.Gln610=
  • NP_001394661.1:p.Gln610=
  • NP_001394662.1:p.Gln610=
  • NP_001394663.1:p.Gln610=
  • NP_001394664.1:p.Gln610=
  • NP_001394665.1:p.Gln610=
  • NP_001394666.1:p.Gln610=
  • NP_001394667.1:p.Gln610=
  • NP_001394668.1:p.Gln610=
  • NP_001394669.1:p.Gln609=
  • NP_001394670.1:p.Gln609=
  • NP_001394671.1:p.Gln609=
  • NP_001394672.1:p.Gln609=
  • NP_001394673.1:p.Gln609=
  • NP_001394674.1:p.Gln609=
  • NP_001394675.1:p.Gln609=
  • NP_001394676.1:p.Gln609=
  • NP_001394677.1:p.Gln609=
  • NP_001394678.1:p.Gln609=
  • NP_001394679.1:p.Gln610=
  • NP_001394680.1:p.Gln610=
  • NP_001394681.1:p.Gln610=
  • NP_001394767.1:p.Gln609=
  • NP_001394768.1:p.Gln609=
  • NP_001394770.1:p.Gln609=
  • NP_001394771.1:p.Gln609=
  • NP_001394772.1:p.Gln609=
  • NP_001394773.1:p.Gln609=
  • NP_001394774.1:p.Gln609=
  • NP_001394775.1:p.Gln609=
  • NP_001394776.1:p.Gln609=
  • NP_001394777.1:p.Gln609=
  • NP_001394778.1:p.Gln609=
  • NP_001394779.1:p.Gln610=
  • NP_001394780.1:p.Gln610=
  • NP_001394781.1:p.Gln610=
  • NP_001394782.1:p.Gln586=
  • NP_001394783.1:p.Gln657=
  • NP_001394787.1:p.Gln657=
  • NP_001394788.1:p.Gln657=
  • NP_001394789.1:p.Gln656=
  • NP_001394790.1:p.Gln656=
  • NP_001394791.1:p.Gln590=
  • NP_001394792.1:p.Gln616=
  • NP_001394803.1:p.Gln589=
  • NP_001394804.1:p.Gln589=
  • NP_001394808.1:p.Gln587=
  • NP_001394810.1:p.Gln587=
  • NP_001394811.1:p.Gln587=
  • NP_001394813.1:p.Gln587=
  • NP_001394814.1:p.Gln587=
  • NP_001394815.1:p.Gln587=
  • NP_001394816.1:p.Gln587=
  • NP_001394818.1:p.Gln587=
  • NP_001394823.1:p.Gln586=
  • NP_001394824.1:p.Gln586=
  • NP_001394825.1:p.Gln586=
  • NP_001394826.1:p.Gln586=
  • NP_001394827.1:p.Gln586=
  • NP_001394828.1:p.Gln586=
  • NP_001394829.1:p.Gln587=
  • NP_001394831.1:p.Gln587=
  • NP_001394833.1:p.Gln587=
  • NP_001394835.1:p.Gln587=
  • NP_001394836.1:p.Gln587=
  • NP_001394837.1:p.Gln587=
  • NP_001394838.1:p.Gln587=
  • NP_001394839.1:p.Gln587=
  • NP_001394844.1:p.Gln586=
  • NP_001394845.1:p.Gln586=
  • NP_001394846.1:p.Gln586=
  • NP_001394847.1:p.Gln586=
  • NP_001394848.1:p.Gln616=
  • NP_001394849.1:p.Gln569=
  • NP_001394850.1:p.Gln569=
  • NP_001394851.1:p.Gln569=
  • NP_001394852.1:p.Gln569=
  • NP_001394853.1:p.Gln569=
  • NP_001394854.1:p.Gln569=
  • NP_001394855.1:p.Gln569=
  • NP_001394856.1:p.Gln569=
  • NP_001394857.1:p.Gln569=
  • NP_001394858.1:p.Gln569=
  • NP_001394859.1:p.Gln568=
  • NP_001394860.1:p.Gln568=
  • NP_001394861.1:p.Gln568=
  • NP_001394862.1:p.Gln569=
  • NP_001394863.1:p.Gln568=
  • NP_001394864.1:p.Gln569=
  • NP_001394865.1:p.Gln568=
  • NP_001394866.1:p.Gln616=
  • NP_001394867.1:p.Gln616=
  • NP_001394868.1:p.Gln616=
  • NP_001394869.1:p.Gln615=
  • NP_001394870.1:p.Gln615=
  • NP_001394871.1:p.Gln610=
  • NP_001394872.1:p.Gln609=
  • NP_001394873.1:p.Gln610=
  • NP_001394874.1:p.Gln610=
  • NP_001394875.1:p.Gln546=
  • NP_001394876.1:p.Gln546=
  • NP_001394877.1:p.Gln546=
  • NP_001394878.1:p.Gln546=
  • NP_001394879.1:p.Gln546=
  • NP_001394880.1:p.Gln546=
  • NP_001394881.1:p.Gln546=
  • NP_001394882.1:p.Gln546=
  • NP_001394883.1:p.Gln545=
  • NP_001394884.1:p.Gln545=
  • NP_001394885.1:p.Gln545=
  • NP_001394886.1:p.Gln546=
  • NP_001394887.1:p.Gln545=
  • NP_001394888.1:p.Gln530=
  • NP_001394889.1:p.Gln530=
  • NP_001394891.1:p.Gln529=
  • NP_001394892.1:p.Gln530=
  • NP_001394893.1:p.Gln609=
  • NP_001394894.1:p.Gln489=
  • NP_001394895.1:p.Gln361=
  • NP_001394896.1:p.Gln361=
  • NP_009225.1:p.Gln657=
  • NP_009225.1:p.Gln657=
  • NP_009228.2:p.Gln610=
  • NP_009231.2:p.Gln657=
  • LRG_292t1:c.1971A>G
  • LRG_292:g.124424A>G
  • LRG_292p1:p.Gln657=
  • NC_000017.10:g.41245577T>C
  • NM_007294.2:c.1971A>G
  • NM_007294.3:c.1971A>G
  • NM_007294.4:c.1971A>G
  • NM_007299.3:c.787+1184A>G
  • NM_007300.3:c.1971A>G
  • NR_027676.2:n.2148A>G
  • U14680.1:n.2090A>G
  • p.Q657Q
Links:
Breast Cancer Information Core (BIC) (BRCA1): 2090&base_change=A to G; dbSNP: rs28897679
NCBI 1000 Genomes Browser:
rs28897679
Molecular consequence:
  • NM_001407968.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.790+1181A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.778+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.709+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.709+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.709+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.706+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.709+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.709+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.706+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.670+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.670+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.670+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.667+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.670+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.670+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.667+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.667+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.661+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.661+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.661+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.661+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.664+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.661+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.661+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.661+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.661+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.661+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.652+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.643+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.643+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.643+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.643+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.643+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.646+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.643+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.784+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.586+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.583+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.586+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.574+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.574+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.574+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.548-2528A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.545-2528A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.523+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.523+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.523+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.523+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.523+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.523+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.454+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.520+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.520+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.520+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.460+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.460+2286A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.451+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.451+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.406+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.404-2528A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.283+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.577+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.787+1184A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407581.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407582.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407583.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407585.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407587.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407590.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407591.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407593.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407594.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407596.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407597.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407598.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407602.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407603.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407605.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407610.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407611.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407612.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407613.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407614.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407615.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407616.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407617.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407618.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407619.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407620.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407621.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407622.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407623.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407624.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407625.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407626.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407627.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407628.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407629.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407630.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407631.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407632.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407633.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407634.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407635.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407636.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407637.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407638.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407639.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407640.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407641.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407642.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407644.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407645.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407646.1:c.1962A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407647.1:c.1962A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407648.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407649.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407652.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407653.1:c.1893A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407654.1:c.1893A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407655.1:c.1893A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407656.1:c.1893A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407657.1:c.1893A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407658.1:c.1893A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407659.1:c.1890A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407660.1:c.1890A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407661.1:c.1890A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407662.1:c.1890A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407663.1:c.1893A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407664.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407665.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407666.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407667.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407668.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407669.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407670.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407671.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407672.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407673.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407674.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407675.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407676.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407677.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407678.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407679.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407680.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407681.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407682.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407683.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407684.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407685.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407686.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407687.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407688.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407689.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407690.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407691.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407692.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407694.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407695.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407696.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407697.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407698.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407724.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407725.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407726.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407727.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407728.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407729.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407730.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407731.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407732.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407733.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407734.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407735.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407736.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407737.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407738.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407739.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407740.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407741.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407742.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407743.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407744.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407745.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407746.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407747.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407748.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407749.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407750.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407751.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407752.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407838.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407839.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407841.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407842.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407843.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407844.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407845.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407846.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407847.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407848.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407849.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407850.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407851.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407852.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407853.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407854.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407858.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407859.1:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407860.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407861.1:c.1968A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407862.1:c.1770A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407863.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407874.1:c.1767A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407875.1:c.1767A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407879.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407881.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407882.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407884.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407885.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407886.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407887.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407889.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407894.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407895.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407896.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407897.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407898.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407899.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407900.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407902.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407904.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407906.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407907.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407908.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407909.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407910.1:c.1761A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407915.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407916.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407917.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407918.1:c.1758A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407919.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407920.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407921.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407922.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407923.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407924.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407925.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407926.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407927.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407928.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407929.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407930.1:c.1704A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407931.1:c.1704A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407932.1:c.1704A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407933.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407934.1:c.1704A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407935.1:c.1707A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407936.1:c.1704A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407937.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407938.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407939.1:c.1848A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407940.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407941.1:c.1845A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407942.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407943.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407944.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407945.1:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407946.1:c.1638A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407947.1:c.1638A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407948.1:c.1638A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407949.1:c.1638A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407950.1:c.1638A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407951.1:c.1638A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407952.1:c.1638A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407953.1:c.1638A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407954.1:c.1635A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407955.1:c.1635A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407956.1:c.1635A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407957.1:c.1638A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407958.1:c.1635A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407959.1:c.1590A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407960.1:c.1590A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407962.1:c.1587A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407963.1:c.1590A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407964.1:c.1827A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407965.1:c.1467A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407966.1:c.1083A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001407967.1:c.1083A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_007294.4:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_007297.4:c.1830A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_007300.4:c.1971A>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Malignant tumor of breast
Synonyms:
Malignant breast neoplasm; Cancer breast
Identifiers:
MONDO: MONDO:0007254; MedGen: C0006142

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000591359Department of Pathology and Laboratory Medicine, Sinai Health System - The Canadian Open Genetics Repository (COGR)

See additional submitters

no assertion criteria provided
Benignunknownclinical testing

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownyes0not providednot providednot providednot providedclinical testing

Details of each submission

From Department of Pathology and Laboratory Medicine, Sinai Health System - The Canadian Open Genetics Repository (COGR), SCV000591359.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided0not providednot providedclinical testingnot provided

Description

Borg_2010 Fackenthal_2012

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot provided0not providednot providednot provided

Last Updated: Nov 3, 2024