NM_007294.4(BRCA1):c.2269del (p.Val757fs) AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:: Pathogenic (9 submissions)
Last evaluated:: Apr 22, 2016
Review status:: 3 stars out of maximum of 4 stars
reviewed by expert panel

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:: RCV000031040.23

Allele description [Variation Report for NM_007294.4(BRCA1):c.2269del (p.Val757fs)]

NM_007294.4(BRCA1):c.2269del (p.Val757fs)

Gene:

BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

17q21.31

Genomic location:

Preferred name:

NM_007294.4(BRCA1):c.2269del (p.Val757fs)

HGVS:

NC_000017.10:g.41245279del
NC_000017.11:g.43093264del
NG_005905.2:g.124722del
NM_001407571.1:c.2056del
NM_001407581.1:c.2269del
NM_001407582.1:c.2269del
NM_001407583.1:c.2269del
NM_001407585.1:c.2269del
NM_001407587.1:c.2266del
NM_001407590.1:c.2266del
NM_001407591.1:c.2266del
NM_001407593.1:c.2269del
NM_001407594.1:c.2269del
NM_001407596.1:c.2269del
NM_001407597.1:c.2269del
NM_001407598.1:c.2269del
NM_001407602.1:c.2269del
NM_001407603.1:c.2269del
NM_001407605.1:c.2269del
NM_001407610.1:c.2266del
NM_001407611.1:c.2266del
NM_001407612.1:c.2266del
NM_001407613.1:c.2266del
NM_001407614.1:c.2266del
NM_001407615.1:c.2266del
NM_001407616.1:c.2269del
NM_001407617.1:c.2269del
NM_001407618.1:c.2269del
NM_001407619.1:c.2269del
NM_001407620.1:c.2269del
NM_001407621.1:c.2269del
NM_001407622.1:c.2269del
NM_001407623.1:c.2269del
NM_001407624.1:c.2269del
NM_001407625.1:c.2269del
NM_001407626.1:c.2269del
NM_001407627.1:c.2266del
NM_001407628.1:c.2266del
NM_001407629.1:c.2266del
NM_001407630.1:c.2266del
NM_001407631.1:c.2266del
NM_001407632.1:c.2266del
NM_001407633.1:c.2266del
NM_001407634.1:c.2266del
NM_001407635.1:c.2266del
NM_001407636.1:c.2266del
NM_001407637.1:c.2266del
NM_001407638.1:c.2266del
NM_001407639.1:c.2269del
NM_001407640.1:c.2269del
NM_001407641.1:c.2269del
NM_001407642.1:c.2269del
NM_001407644.1:c.2266del
NM_001407645.1:c.2266del
NM_001407646.1:c.2260del
NM_001407647.1:c.2260del
NM_001407648.1:c.2146del
NM_001407649.1:c.2143del
NM_001407652.1:c.2269del
NM_001407653.1:c.2191del
NM_001407654.1:c.2191del
NM_001407655.1:c.2191del
NM_001407656.1:c.2191del
NM_001407657.1:c.2191del
NM_001407658.1:c.2191del
NM_001407659.1:c.2188del
NM_001407660.1:c.2188del
NM_001407661.1:c.2188del
NM_001407662.1:c.2188del
NM_001407663.1:c.2191del
NM_001407664.1:c.2146del
NM_001407665.1:c.2146del
NM_001407666.1:c.2146del
NM_001407667.1:c.2146del
NM_001407668.1:c.2146del
NM_001407669.1:c.2146del
NM_001407670.1:c.2143del
NM_001407671.1:c.2143del
NM_001407672.1:c.2143del
NM_001407673.1:c.2143del
NM_001407674.1:c.2146del
NM_001407675.1:c.2146del
NM_001407676.1:c.2146del
NM_001407677.1:c.2146del
NM_001407678.1:c.2146del
NM_001407679.1:c.2146del
NM_001407680.1:c.2146del
NM_001407681.1:c.2146del
NM_001407682.1:c.2146del
NM_001407683.1:c.2146del
NM_001407684.1:c.2269del
NM_001407685.1:c.2143del
NM_001407686.1:c.2143del
NM_001407687.1:c.2143del
NM_001407688.1:c.2143del
NM_001407689.1:c.2143del
NM_001407690.1:c.2143del
NM_001407691.1:c.2143del
NM_001407692.1:c.2128del
NM_001407694.1:c.2128del
NM_001407695.1:c.2128del
NM_001407696.1:c.2128del
NM_001407697.1:c.2128del
NM_001407698.1:c.2128del
NM_001407724.1:c.2128del
NM_001407725.1:c.2128del
NM_001407726.1:c.2128del
NM_001407727.1:c.2128del
NM_001407728.1:c.2128del
NM_001407729.1:c.2128del
NM_001407730.1:c.2128del
NM_001407731.1:c.2128del
NM_001407732.1:c.2128del
NM_001407733.1:c.2128del
NM_001407734.1:c.2128del
NM_001407735.1:c.2128del
NM_001407736.1:c.2128del
NM_001407737.1:c.2128del
NM_001407738.1:c.2128del
NM_001407739.1:c.2128del
NM_001407740.1:c.2125del
NM_001407741.1:c.2125del
NM_001407742.1:c.2125del
NM_001407743.1:c.2125del
NM_001407744.1:c.2125del
NM_001407745.1:c.2125del
NM_001407746.1:c.2125del
NM_001407747.1:c.2125del
NM_001407748.1:c.2125del
NM_001407749.1:c.2125del
NM_001407750.1:c.2128del
NM_001407751.1:c.2128del
NM_001407752.1:c.2128del
NM_001407838.1:c.2125del
NM_001407839.1:c.2125del
NM_001407841.1:c.2125del
NM_001407842.1:c.2125del
NM_001407843.1:c.2125del
NM_001407844.1:c.2125del
NM_001407845.1:c.2125del
NM_001407846.1:c.2125del
NM_001407847.1:c.2125del
NM_001407848.1:c.2125del
NM_001407849.1:c.2125del
NM_001407850.1:c.2128del
NM_001407851.1:c.2128del
NM_001407852.1:c.2128del
NM_001407853.1:c.2056del
NM_001407854.1:c.2269del
NM_001407858.1:c.2269del
NM_001407859.1:c.2269del
NM_001407860.1:c.2266del
NM_001407861.1:c.2266del
NM_001407862.1:c.2068del
NM_001407863.1:c.2146del
NM_001407874.1:c.2065del
NM_001407875.1:c.2065del
NM_001407879.1:c.2059del
NM_001407881.1:c.2059del
NM_001407882.1:c.2059del
NM_001407884.1:c.2059del
NM_001407885.1:c.2059del
NM_001407886.1:c.2059del
NM_001407887.1:c.2059del
NM_001407889.1:c.2059del
NM_001407894.1:c.2056del
NM_001407895.1:c.2056del
NM_001407896.1:c.2056del
NM_001407897.1:c.2056del
NM_001407898.1:c.2056del
NM_001407899.1:c.2056del
NM_001407900.1:c.2059del
NM_001407902.1:c.2059del
NM_001407904.1:c.2059del
NM_001407906.1:c.2059del
NM_001407907.1:c.2059del
NM_001407908.1:c.2059del
NM_001407909.1:c.2059del
NM_001407910.1:c.2059del
NM_001407915.1:c.2056del
NM_001407916.1:c.2056del
NM_001407917.1:c.2056del
NM_001407918.1:c.2056del
NM_001407919.1:c.2146del
NM_001407920.1:c.2005del
NM_001407921.1:c.2005del
NM_001407922.1:c.2005del
NM_001407923.1:c.2005del
NM_001407924.1:c.2005del
NM_001407925.1:c.2005del
NM_001407926.1:c.2005del
NM_001407927.1:c.2005del
NM_001407928.1:c.2005del
NM_001407929.1:c.2005del
NM_001407930.1:c.2002del
NM_001407931.1:c.2002del
NM_001407932.1:c.2002del
NM_001407933.1:c.2005del
NM_001407934.1:c.2002del
NM_001407935.1:c.2005del
NM_001407936.1:c.2002del
NM_001407937.1:c.2146del
NM_001407938.1:c.2146del
NM_001407939.1:c.2146del
NM_001407940.1:c.2143del
NM_001407941.1:c.2143del
NM_001407942.1:c.2128del
NM_001407943.1:c.2125del
NM_001407944.1:c.2128del
NM_001407945.1:c.2128del
NM_001407946.1:c.1936del
NM_001407947.1:c.1936del
NM_001407948.1:c.1936del
NM_001407949.1:c.1936del
NM_001407950.1:c.1936del
NM_001407951.1:c.1936del
NM_001407952.1:c.1936del
NM_001407953.1:c.1936del
NM_001407954.1:c.1933del
NM_001407955.1:c.1933del
NM_001407956.1:c.1933del
NM_001407957.1:c.1936del
NM_001407958.1:c.1933del
NM_001407959.1:c.1888del
NM_001407960.1:c.1888del
NM_001407962.1:c.1885del
NM_001407963.1:c.1888del
NM_001407964.1:c.2125del
NM_001407965.1:c.1765del
NM_001407966.1:c.1381del
NM_001407967.1:c.1381del
NM_001407968.1:c.788-1123del
NM_001407969.1:c.788-1123del
NM_001407970.1:c.787+1482del
NM_001407971.1:c.787+1482del
NM_001407972.1:c.784+1482del
NM_001407973.1:c.787+1482del
NM_001407974.1:c.787+1482del
NM_001407975.1:c.787+1482del
NM_001407976.1:c.787+1482del
NM_001407977.1:c.787+1482del
NM_001407978.1:c.787+1482del
NM_001407979.1:c.787+1482del
NM_001407980.1:c.787+1482del
NM_001407981.1:c.787+1482del
NM_001407982.1:c.787+1482del
NM_001407983.1:c.787+1482del
NM_001407984.1:c.784+1482del
NM_001407985.1:c.784+1482del
NM_001407986.1:c.784+1482del
NM_001407990.1:c.787+1482del
NM_001407991.1:c.784+1482del
NM_001407992.1:c.784+1482del
NM_001407993.1:c.787+1482del
NM_001408392.1:c.784+1482del
NM_001408396.1:c.784+1482del
NM_001408397.1:c.784+1482del
NM_001408398.1:c.784+1482del
NM_001408399.1:c.784+1482del
NM_001408400.1:c.784+1482del
NM_001408401.1:c.784+1482del
NM_001408402.1:c.784+1482del
NM_001408403.1:c.787+1482del
NM_001408404.1:c.787+1482del
NM_001408406.1:c.790+1479del
NM_001408407.1:c.784+1482del
NM_001408408.1:c.778+1482del
NM_001408409.1:c.709+1482del
NM_001408410.1:c.646+1482del
NM_001408411.1:c.709+1482del
NM_001408412.1:c.709+1482del
NM_001408413.1:c.706+1482del
NM_001408414.1:c.709+1482del
NM_001408415.1:c.709+1482del
NM_001408416.1:c.706+1482del
NM_001408418.1:c.671-2230del
NM_001408419.1:c.671-2230del
NM_001408420.1:c.671-2230del
NM_001408421.1:c.668-2230del
NM_001408422.1:c.671-2230del
NM_001408423.1:c.671-2230del
NM_001408424.1:c.668-2230del
NM_001408425.1:c.664+1482del
NM_001408426.1:c.664+1482del
NM_001408427.1:c.664+1482del
NM_001408428.1:c.664+1482del
NM_001408429.1:c.664+1482del
NM_001408430.1:c.664+1482del
NM_001408431.1:c.668-2230del
NM_001408432.1:c.661+1482del
NM_001408433.1:c.661+1482del
NM_001408434.1:c.661+1482del
NM_001408435.1:c.661+1482del
NM_001408436.1:c.664+1482del
NM_001408437.1:c.664+1482del
NM_001408438.1:c.664+1482del
NM_001408439.1:c.664+1482del
NM_001408440.1:c.664+1482del
NM_001408441.1:c.664+1482del
NM_001408442.1:c.664+1482del
NM_001408443.1:c.664+1482del
NM_001408444.1:c.664+1482del
NM_001408445.1:c.661+1482del
NM_001408446.1:c.661+1482del
NM_001408447.1:c.661+1482del
NM_001408448.1:c.661+1482del
NM_001408450.1:c.661+1482del
NM_001408451.1:c.652+1482del
NM_001408452.1:c.646+1482del
NM_001408453.1:c.646+1482del
NM_001408454.1:c.646+1482del
NM_001408455.1:c.646+1482del
NM_001408456.1:c.646+1482del
NM_001408457.1:c.646+1482del
NM_001408458.1:c.646+1482del
NM_001408459.1:c.646+1482del
NM_001408460.1:c.646+1482del
NM_001408461.1:c.646+1482del
NM_001408462.1:c.643+1482del
NM_001408463.1:c.643+1482del
NM_001408464.1:c.643+1482del
NM_001408465.1:c.643+1482del
NM_001408466.1:c.646+1482del
NM_001408467.1:c.646+1482del
NM_001408468.1:c.643+1482del
NM_001408469.1:c.646+1482del
NM_001408470.1:c.643+1482del
NM_001408472.1:c.787+1482del
NM_001408473.1:c.784+1482del
NM_001408474.1:c.586+1482del
NM_001408475.1:c.583+1482del
NM_001408476.1:c.586+1482del
NM_001408478.1:c.577+1482del
NM_001408479.1:c.577+1482del
NM_001408480.1:c.577+1482del
NM_001408481.1:c.577+1482del
NM_001408482.1:c.577+1482del
NM_001408483.1:c.577+1482del
NM_001408484.1:c.577+1482del
NM_001408485.1:c.577+1482del
NM_001408489.1:c.577+1482del
NM_001408490.1:c.574+1482del
NM_001408491.1:c.574+1482del
NM_001408492.1:c.577+1482del
NM_001408493.1:c.574+1482del
NM_001408494.1:c.548-2230del
NM_001408495.1:c.545-2230del
NM_001408496.1:c.523+1482del
NM_001408497.1:c.523+1482del
NM_001408498.1:c.523+1482del
NM_001408499.1:c.523+1482del
NM_001408500.1:c.523+1482del
NM_001408501.1:c.523+1482del
NM_001408502.1:c.454+1482del
NM_001408503.1:c.520+1482del
NM_001408504.1:c.520+1482del
NM_001408505.1:c.520+1482del
NM_001408506.1:c.461-2230del
NM_001408507.1:c.461-2230del
NM_001408508.1:c.451+1482del
NM_001408509.1:c.451+1482del
NM_001408510.1:c.406+1482del
NM_001408511.1:c.404-2230del
NM_001408512.1:c.283+1482del
NM_001408513.1:c.577+1482del
NM_001408514.1:c.577+1482del
NM_007294.4:c.2269delMANE SELECT
NM_007297.4:c.2128del
NM_007298.4:c.787+1482del
NM_007299.4:c.787+1482del
NM_007300.4:c.2269del
NP_001394500.1:p.Val686fs
NP_001394510.1:p.Val757fs
NP_001394511.1:p.Val757fs
NP_001394512.1:p.Val757fs
NP_001394514.1:p.Val757fs
NP_001394516.1:p.Val756fs
NP_001394519.1:p.Val756fs
NP_001394520.1:p.Val756fs
NP_001394522.1:p.Val757fs
NP_001394523.1:p.Val757fs
NP_001394525.1:p.Val757fs
NP_001394526.1:p.Val757fs
NP_001394527.1:p.Val757fs
NP_001394531.1:p.Val757fs
NP_001394532.1:p.Val757fs
NP_001394534.1:p.Val757fs
NP_001394539.1:p.Val756fs
NP_001394540.1:p.Val756fs
NP_001394541.1:p.Val756fs
NP_001394542.1:p.Val756fs
NP_001394543.1:p.Val756fs
NP_001394544.1:p.Val756fs
NP_001394545.1:p.Val757fs
NP_001394546.1:p.Val757fs
NP_001394547.1:p.Val757fs
NP_001394548.1:p.Val757fs
NP_001394549.1:p.Val757fs
NP_001394550.1:p.Val757fs
NP_001394551.1:p.Val757fs
NP_001394552.1:p.Val757fs
NP_001394553.1:p.Val757fs
NP_001394554.1:p.Val757fs
NP_001394555.1:p.Val757fs
NP_001394556.1:p.Val756fs
NP_001394557.1:p.Val756fs
NP_001394558.1:p.Val756fs
NP_001394559.1:p.Val756fs
NP_001394560.1:p.Val756fs
NP_001394561.1:p.Val756fs
NP_001394562.1:p.Val756fs
NP_001394563.1:p.Val756fs
NP_001394564.1:p.Val756fs
NP_001394565.1:p.Val756fs
NP_001394566.1:p.Val756fs
NP_001394567.1:p.Val756fs
NP_001394568.1:p.Val757fs
NP_001394569.1:p.Val757fs
NP_001394570.1:p.Val757fs
NP_001394571.1:p.Val757fs
NP_001394573.1:p.Val756fs
NP_001394574.1:p.Val756fs
NP_001394575.1:p.Val754fs
NP_001394576.1:p.Val754fs
NP_001394577.1:p.Val716fs
NP_001394578.1:p.Val715fs
NP_001394581.1:p.Val757fs
NP_001394582.1:p.Val731fs
NP_001394583.1:p.Val731fs
NP_001394584.1:p.Val731fs
NP_001394585.1:p.Val731fs
NP_001394586.1:p.Val731fs
NP_001394587.1:p.Val731fs
NP_001394588.1:p.Val730fs
NP_001394589.1:p.Val730fs
NP_001394590.1:p.Val730fs
NP_001394591.1:p.Val730fs
NP_001394592.1:p.Val731fs
NP_001394593.1:p.Val716fs
NP_001394594.1:p.Val716fs
NP_001394595.1:p.Val716fs
NP_001394596.1:p.Val716fs
NP_001394597.1:p.Val716fs
NP_001394598.1:p.Val716fs
NP_001394599.1:p.Val715fs
NP_001394600.1:p.Val715fs
NP_001394601.1:p.Val715fs
NP_001394602.1:p.Val715fs
NP_001394603.1:p.Val716fs
NP_001394604.1:p.Val716fs
NP_001394605.1:p.Val716fs
NP_001394606.1:p.Val716fs
NP_001394607.1:p.Val716fs
NP_001394608.1:p.Val716fs
NP_001394609.1:p.Val716fs
NP_001394610.1:p.Val716fs
NP_001394611.1:p.Val716fs
NP_001394612.1:p.Val716fs
NP_001394613.1:p.Val757fs
NP_001394614.1:p.Val715fs
NP_001394615.1:p.Val715fs
NP_001394616.1:p.Val715fs
NP_001394617.1:p.Val715fs
NP_001394618.1:p.Val715fs
NP_001394619.1:p.Val715fs
NP_001394620.1:p.Val715fs
NP_001394621.1:p.Val710fs
NP_001394623.1:p.Val710fs
NP_001394624.1:p.Val710fs
NP_001394625.1:p.Val710fs
NP_001394626.1:p.Val710fs
NP_001394627.1:p.Val710fs
NP_001394653.1:p.Val710fs
NP_001394654.1:p.Val710fs
NP_001394655.1:p.Val710fs
NP_001394656.1:p.Val710fs
NP_001394657.1:p.Val710fs
NP_001394658.1:p.Val710fs
NP_001394659.1:p.Val710fs
NP_001394660.1:p.Val710fs
NP_001394661.1:p.Val710fs
NP_001394662.1:p.Val710fs
NP_001394663.1:p.Val710fs
NP_001394664.1:p.Val710fs
NP_001394665.1:p.Val710fs
NP_001394666.1:p.Val710fs
NP_001394667.1:p.Val710fs
NP_001394668.1:p.Val710fs
NP_001394669.1:p.Val709fs
NP_001394670.1:p.Val709fs
NP_001394671.1:p.Val709fs
NP_001394672.1:p.Val709fs
NP_001394673.1:p.Val709fs
NP_001394674.1:p.Val709fs
NP_001394675.1:p.Val709fs
NP_001394676.1:p.Val709fs
NP_001394677.1:p.Val709fs
NP_001394678.1:p.Val709fs
NP_001394679.1:p.Val710fs
NP_001394680.1:p.Val710fs
NP_001394681.1:p.Val710fs
NP_001394767.1:p.Val709fs
NP_001394768.1:p.Val709fs
NP_001394770.1:p.Val709fs
NP_001394771.1:p.Val709fs
NP_001394772.1:p.Val709fs
NP_001394773.1:p.Val709fs
NP_001394774.1:p.Val709fs
NP_001394775.1:p.Val709fs
NP_001394776.1:p.Val709fs
NP_001394777.1:p.Val709fs
NP_001394778.1:p.Val709fs
NP_001394779.1:p.Val710fs
NP_001394780.1:p.Val710fs
NP_001394781.1:p.Val710fs
NP_001394782.1:p.Val686fs
NP_001394783.1:p.Val757fs
NP_001394787.1:p.Val757fs
NP_001394788.1:p.Val757fs
NP_001394789.1:p.Val756fs
NP_001394790.1:p.Val756fs
NP_001394791.1:p.Val690fs
NP_001394792.1:p.Val716fs
NP_001394803.1:p.Val689fs
NP_001394804.1:p.Val689fs
NP_001394808.1:p.Val687fs
NP_001394810.1:p.Val687fs
NP_001394811.1:p.Val687fs
NP_001394813.1:p.Val687fs
NP_001394814.1:p.Val687fs
NP_001394815.1:p.Val687fs
NP_001394816.1:p.Val687fs
NP_001394818.1:p.Val687fs
NP_001394823.1:p.Val686fs
NP_001394824.1:p.Val686fs
NP_001394825.1:p.Val686fs
NP_001394826.1:p.Val686fs
NP_001394827.1:p.Val686fs
NP_001394828.1:p.Val686fs
NP_001394829.1:p.Val687fs
NP_001394831.1:p.Val687fs
NP_001394833.1:p.Val687fs
NP_001394835.1:p.Val687fs
NP_001394836.1:p.Val687fs
NP_001394837.1:p.Val687fs
NP_001394838.1:p.Val687fs
NP_001394839.1:p.Val687fs
NP_001394844.1:p.Val686fs
NP_001394845.1:p.Val686fs
NP_001394846.1:p.Val686fs
NP_001394847.1:p.Val686fs
NP_001394848.1:p.Val716fs
NP_001394849.1:p.Val669fs
NP_001394850.1:p.Val669fs
NP_001394851.1:p.Val669fs
NP_001394852.1:p.Val669fs
NP_001394853.1:p.Val669fs
NP_001394854.1:p.Val669fs
NP_001394855.1:p.Val669fs
NP_001394856.1:p.Val669fs
NP_001394857.1:p.Val669fs
NP_001394858.1:p.Val669fs
NP_001394859.1:p.Val668fs
NP_001394860.1:p.Val668fs
NP_001394861.1:p.Val668fs
NP_001394862.1:p.Val669fs
NP_001394863.1:p.Val668fs
NP_001394864.1:p.Val669fs
NP_001394865.1:p.Val668fs
NP_001394866.1:p.Val716fs
NP_001394867.1:p.Val716fs
NP_001394868.1:p.Val716fs
NP_001394869.1:p.Val715fs
NP_001394870.1:p.Val715fs
NP_001394871.1:p.Val710fs
NP_001394872.1:p.Val709fs
NP_001394873.1:p.Val710fs
NP_001394874.1:p.Val710fs
NP_001394875.1:p.Val646fs
NP_001394876.1:p.Val646fs
NP_001394877.1:p.Val646fs
NP_001394878.1:p.Val646fs
NP_001394879.1:p.Val646fs
NP_001394880.1:p.Val646fs
NP_001394881.1:p.Val646fs
NP_001394882.1:p.Val646fs
NP_001394883.1:p.Val645fs
NP_001394884.1:p.Val645fs
NP_001394885.1:p.Val645fs
NP_001394886.1:p.Val646fs
NP_001394887.1:p.Val645fs
NP_001394888.1:p.Val630fs
NP_001394889.1:p.Val630fs
NP_001394891.1:p.Val629fs
NP_001394892.1:p.Val630fs
NP_001394893.1:p.Val709fs
NP_001394894.1:p.Val589fs
NP_001394895.1:p.Val461fs
NP_001394896.1:p.Val461fs
NP_009225.1:p.Val757Phefs
NP_009225.1:p.Val757fs
NP_009228.2:p.Val710fs
NP_009231.2:p.Val757fs
LRG_292t1:c.2267del
LRG_292:g.124722del
LRG_292p1:p.Val757Phefs
NC_000017.10:g.41245279del
NC_000017.10:g.41245279delC
NC_000017.10:g.41245281del
NC_000017.10:g.41245281del
NM_007294.3:c.2267delG
NM_007294.3:c.2269delG
NM_007294.4:c.2269del
NM_007300.3:c.2269delG
NR_027676.1:n.2403delG
U14680.1:n.2388delG

Nucleotide change:

2388delG

Protein change:

V461fs

Links:

Breast Cancer Information Core (BIC) (BRCA1): 2388&base_change=del G; dbSNP: rs80357583

NCBI 1000 Genomes Browser:

rs80357583

Molecular consequence:

NM_001407571.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407581.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407582.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407583.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407585.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407587.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407590.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407591.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407593.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407594.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407596.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407597.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407598.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407602.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407603.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407605.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407610.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407611.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407612.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407613.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407614.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407615.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407616.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407617.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407618.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407619.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407620.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407621.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407622.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407623.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407624.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407625.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407626.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407627.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407628.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407629.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407630.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407631.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407632.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407633.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407634.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407635.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407636.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407637.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407638.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407639.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407640.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407641.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407642.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407644.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407645.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407646.1:c.2260del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407647.1:c.2260del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407648.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407649.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407652.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407653.1:c.2191del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407654.1:c.2191del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407655.1:c.2191del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407656.1:c.2191del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407657.1:c.2191del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407658.1:c.2191del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407659.1:c.2188del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407660.1:c.2188del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407661.1:c.2188del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407662.1:c.2188del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407663.1:c.2191del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407664.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407665.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407666.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407667.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407668.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407669.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407670.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407671.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407672.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407673.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407674.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407675.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407676.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407677.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407678.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407679.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407680.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407681.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407682.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407683.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407684.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407685.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407686.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407687.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407688.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407689.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407690.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407691.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407692.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407694.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407695.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407696.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407697.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407698.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407724.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407725.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407726.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407727.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407728.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407729.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407730.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407731.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407732.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407733.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407734.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407735.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407736.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407737.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407738.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407739.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407740.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407741.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407742.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407743.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407744.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407745.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407746.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407747.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407748.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407749.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407750.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407751.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407752.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407838.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407839.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407841.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407842.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407843.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407844.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407845.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407846.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407847.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407848.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407849.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407850.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407851.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407852.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407853.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407854.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407858.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407859.1:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407860.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407861.1:c.2266del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407862.1:c.2068del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407863.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407874.1:c.2065del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407875.1:c.2065del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407879.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407881.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407882.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407884.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407885.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407886.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407887.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407889.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407894.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407895.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407896.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407897.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407898.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407899.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407900.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407902.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407904.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407906.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407907.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407908.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407909.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407910.1:c.2059del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407915.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407916.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407917.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407918.1:c.2056del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407919.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407920.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407921.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407922.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407923.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407924.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407925.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407926.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407927.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407928.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407929.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407930.1:c.2002del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407931.1:c.2002del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407932.1:c.2002del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407933.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407934.1:c.2002del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407935.1:c.2005del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407936.1:c.2002del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407937.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407938.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407939.1:c.2146del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407940.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407941.1:c.2143del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407942.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407943.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407944.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407945.1:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407946.1:c.1936del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407947.1:c.1936del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407948.1:c.1936del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407949.1:c.1936del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407950.1:c.1936del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407951.1:c.1936del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407952.1:c.1936del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407953.1:c.1936del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407954.1:c.1933del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407955.1:c.1933del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407956.1:c.1933del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407957.1:c.1936del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407958.1:c.1933del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407959.1:c.1888del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407960.1:c.1888del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407962.1:c.1885del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407963.1:c.1888del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407964.1:c.2125del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407965.1:c.1765del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407966.1:c.1381del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407967.1:c.1381del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_007294.4:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_007297.4:c.2128del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_007300.4:c.2269del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001407968.1:c.788-1123del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407969.1:c.788-1123del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407970.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407971.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407972.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407973.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407974.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407975.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407976.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407977.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407978.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407979.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407980.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407981.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407982.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407983.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407984.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407985.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407986.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407990.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407991.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407992.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001407993.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408392.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408396.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408397.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408398.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408399.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408400.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408401.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408402.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408403.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408404.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408406.1:c.790+1479del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408407.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408408.1:c.778+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408409.1:c.709+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408410.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408411.1:c.709+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408412.1:c.709+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408413.1:c.706+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408414.1:c.709+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408415.1:c.709+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408416.1:c.706+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408418.1:c.671-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408419.1:c.671-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408420.1:c.671-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408421.1:c.668-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408422.1:c.671-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408423.1:c.671-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408424.1:c.668-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408425.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408426.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408427.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408428.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408429.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408430.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408431.1:c.668-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408432.1:c.661+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408433.1:c.661+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408434.1:c.661+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408435.1:c.661+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408436.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408437.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408438.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408439.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408440.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408441.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408442.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408443.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408444.1:c.664+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408445.1:c.661+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408446.1:c.661+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408447.1:c.661+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408448.1:c.661+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408450.1:c.661+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408451.1:c.652+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408452.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408453.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408454.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408455.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408456.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408457.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408458.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408459.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408460.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408461.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408462.1:c.643+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408463.1:c.643+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408464.1:c.643+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408465.1:c.643+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408466.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408467.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408468.1:c.643+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408469.1:c.646+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408470.1:c.643+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408472.1:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408473.1:c.784+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408474.1:c.586+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408475.1:c.583+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408476.1:c.586+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408478.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408479.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408480.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408481.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408482.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408483.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408484.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408485.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408489.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408490.1:c.574+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408491.1:c.574+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408492.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408493.1:c.574+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408494.1:c.548-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408495.1:c.545-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408496.1:c.523+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408497.1:c.523+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408498.1:c.523+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408499.1:c.523+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408500.1:c.523+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408501.1:c.523+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408502.1:c.454+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408503.1:c.520+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408504.1:c.520+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408505.1:c.520+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408506.1:c.461-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408507.1:c.461-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408508.1:c.451+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408509.1:c.451+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408510.1:c.406+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408511.1:c.404-2230del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408512.1:c.283+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408513.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_001408514.1:c.577+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_007298.4:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]
NM_007299.4:c.787+1482del - intron variant - [Sequence Ontology: SO:0001627]

Observations:

Condition(s)

Name:: Breast-ovarian cancer, familial, susceptibility to, 1 (BROVCA1)
Synonyms:: OVARIAN CANCER, SUSCEPTIBILITY TO; Breast cancer, familial 1
Identifiers:: MONDO: MONDO:0011450; MedGen: C2676676; Orphanet: 145; OMIM: 604370

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000053634	Sharing Clinical Reports Project (SCRP)	no assertion criteria provided	Pathogenic (Dec 14, 2009)	germline	clinical testing
SCV000144362	Breast Cancer Information Core (BIC) (BRCA1)	no assertion criteria provided	Pathogenic (May 29, 2002)	germline	clinical testing
SCV000282276	Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA)	reviewed by expert panel (ENIGMA BRCA1/2 Classification Criteria (2015))	Pathogenic (Apr 22, 2016)	germline	curation	ENIGMA BRCA1/2 Classification Criteria (2015), Citation Link,
SCV000325310	Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), c/o University of Cambridge	criteria provided, single submitter (CIMBA Mutation Classification guidelines May 2016)	Pathogenic (Oct 2, 2015)	germline	clinical testing	CIMBA_Mutation_Classification_guidelines_May16.pdf, Citation Link,
SCV001499618	Department of Molecular Diagnostics, Institute of Oncology Ljubljana	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Apr 2, 2020)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002762796	Centre for Mendelian Genomics, University Medical Centre Ljubljana	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Dec 9, 2022)	germline	research	PubMed (1) [See all records that cite this PMID]
SCV003927258	KCCC/NGS Laboratory, Kuwait Cancer Control Center	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (May 31, 2023)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV004211736	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Jan 10, 2024)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV004244097	BRCAlab, Lund University	no assertion criteria provided	Pathogenic (Mar 2, 2020)	germline	clinical testing

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	no	not provided	not provided	not provided	not provided	not provided	research
not provided	germline	yes	7	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	not provided	39	not provided	not provided	not provided	clinical testing, curation
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	not provided	1	not provided	not provided	1	not provided	clinical testing
not provided	unknown	yes	1	not provided	not provided	not provided	not provided	clinical testing
Caucasian	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing
Pakistani	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing
Western European	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Sharing Clinical Reports Project (SCRP), SCV000053634.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	not provided	1	not provided	not provided		not provided	not provided	not provided	not provided

From Breast Cancer Information Core (BIC) (BRCA1), SCV000144362.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	7	not provided	not provided	clinical testing	not provided
2	Caucasian	1	not provided	not provided	clinical testing	not provided
3	Pakistani	1	not provided	not provided	clinical testing	not provided
4	Western European	1	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		7	not provided	not provided	not provided
2	germline	yes	not provided	not provided	not provided		1	not provided	not provided	not provided
3	germline	yes	not provided	not provided	not provided		1	not provided	not provided	not provided
4	germline	yes	not provided	not provided	not provided		1	not provided	not provided	not provided

From Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA), SCV000282276.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	curation	not provided

Description

Variant allele predicted to encode a truncated non-functional protein.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), c/o University of Cambridge, SCV000325310.4

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	39	not provided

From Department of Molecular Diagnostics, Institute of Oncology Ljubljana, SCV001499618.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Centre for Mendelian Genomics, University Medical Centre Ljubljana, SCV002762796.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	research	PubMed (1)

Description

PVS1, PS4_STR PM2_SUP

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From KCCC/NGS Laboratory, Kuwait Cancer Control Center, SCV003927258.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1		1	not provided	not provided	clinical testing	PubMed (1)

Description

A known pathogenic variant was detected in the BRCA1 gene (p.Val757fs). This sequence change creates a premature translational stop signal (p.Val757Phefs*8) 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). This variant is present in population databases (rs80357583, gnomAD 0.0009%). This premature translational stop signal has been observed in individual(s) with breast and/or ovarian cancer (PMID: 9150149, 25863477, 26306726, 27553291). This variant is also known as 2388delG. ClinVar contains an entry for this variant (Variation ID: 37459). For these reasons, this variant has been classified as Pathogenic.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	yes	not provided	not provided	not provided		1	not provided	not provided	not provided

From Baylor Genetics, SCV004211736.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From BRCAlab, Lund University, SCV004244097.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 24, 2024

Relating variation to medicine