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NM_007294.4(BRCA1):c.5365G>T (p.Ala1789Ser) AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:
Conflicting interpretations of pathogenicity (4 submissions)
Last evaluated:
May 9, 2017
Review status:
criteria provided, conflicting classifications
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000112629.16

Allele description [Variation Report for NM_007294.4(BRCA1):c.5365G>T (p.Ala1789Ser)]

NM_007294.4(BRCA1):c.5365G>T (p.Ala1789Ser)

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.5365G>T (p.Ala1789Ser)
HGVS:
  • NC_000017.11:g.43049162C>A
  • NG_005905.2:g.168822G>T
  • NM_001407571.1:c.5152G>T
  • NM_001407581.1:c.5431G>T
  • NM_001407582.1:c.5431G>T
  • NM_001407583.1:c.5428G>T
  • NM_001407585.1:c.5428G>T
  • NM_001407587.1:c.5428G>T
  • NM_001407590.1:c.5425G>T
  • NM_001407591.1:c.5425G>T
  • NM_001407593.1:c.5365G>T
  • NM_001407594.1:c.5365G>T
  • NM_001407596.1:c.5365G>T
  • NM_001407597.1:c.5365G>T
  • NM_001407598.1:c.5365G>T
  • NM_001407602.1:c.5365G>T
  • NM_001407603.1:c.5365G>T
  • NM_001407605.1:c.5365G>T
  • NM_001407610.1:c.5362G>T
  • NM_001407611.1:c.5362G>T
  • NM_001407612.1:c.5362G>T
  • NM_001407613.1:c.5362G>T
  • NM_001407614.1:c.5362G>T
  • NM_001407615.1:c.5362G>T
  • NM_001407616.1:c.5362G>T
  • NM_001407617.1:c.5362G>T
  • NM_001407618.1:c.5362G>T
  • NM_001407619.1:c.5362G>T
  • NM_001407620.1:c.5362G>T
  • NM_001407621.1:c.5362G>T
  • NM_001407622.1:c.5362G>T
  • NM_001407623.1:c.5362G>T
  • NM_001407624.1:c.5362G>T
  • NM_001407625.1:c.5362G>T
  • NM_001407626.1:c.5362G>T
  • NM_001407627.1:c.5359G>T
  • NM_001407628.1:c.5359G>T
  • NM_001407629.1:c.5359G>T
  • NM_001407630.1:c.5359G>T
  • NM_001407631.1:c.5359G>T
  • NM_001407632.1:c.5359G>T
  • NM_001407633.1:c.5359G>T
  • NM_001407634.1:c.5359G>T
  • NM_001407635.1:c.5359G>T
  • NM_001407636.1:c.5359G>T
  • NM_001407637.1:c.5359G>T
  • NM_001407638.1:c.5359G>T
  • NM_001407639.1:c.5359G>T
  • NM_001407640.1:c.5359G>T
  • NM_001407641.1:c.5359G>T
  • NM_001407642.1:c.5359G>T
  • NM_001407644.1:c.5356G>T
  • NM_001407645.1:c.5356G>T
  • NM_001407646.1:c.5353G>T
  • NM_001407647.1:c.5350G>T
  • NM_001407648.1:c.5308G>T
  • NM_001407649.1:c.5305G>T
  • NM_001407652.1:c.5287G>T
  • NM_001407653.1:c.5287G>T
  • NM_001407654.1:c.5287G>T
  • NM_001407655.1:c.5287G>T
  • NM_001407656.1:c.5284G>T
  • NM_001407657.1:c.5284G>T
  • NM_001407658.1:c.5284G>T
  • NM_001407659.1:c.5281G>T
  • NM_001407660.1:c.5281G>T
  • NM_001407661.1:c.5281G>T
  • NM_001407662.1:c.5281G>T
  • NM_001407663.1:c.5281G>T
  • NM_001407664.1:c.5242G>T
  • NM_001407665.1:c.5242G>T
  • NM_001407666.1:c.5242G>T
  • NM_001407667.1:c.5242G>T
  • NM_001407668.1:c.5242G>T
  • NM_001407669.1:c.5242G>T
  • NM_001407670.1:c.5239G>T
  • NM_001407671.1:c.5239G>T
  • NM_001407672.1:c.5239G>T
  • NM_001407673.1:c.5239G>T
  • NM_001407674.1:c.5239G>T
  • NM_001407675.1:c.5239G>T
  • NM_001407676.1:c.5239G>T
  • NM_001407677.1:c.5239G>T
  • NM_001407678.1:c.5239G>T
  • NM_001407679.1:c.5239G>T
  • NM_001407680.1:c.5239G>T
  • NM_001407681.1:c.5236G>T
  • NM_001407682.1:c.5236G>T
  • NM_001407683.1:c.5236G>T
  • NM_001407685.1:c.5236G>T
  • NM_001407686.1:c.5236G>T
  • NM_001407687.1:c.5236G>T
  • NM_001407688.1:c.5236G>T
  • NM_001407689.1:c.5236G>T
  • NM_001407690.1:c.5233G>T
  • NM_001407691.1:c.5233G>T
  • NM_001407692.1:c.5224G>T
  • NM_001407694.1:c.5224G>T
  • NM_001407695.1:c.5224G>T
  • NM_001407696.1:c.5224G>T
  • NM_001407697.1:c.5224G>T
  • NM_001407698.1:c.5224G>T
  • NM_001407724.1:c.5224G>T
  • NM_001407725.1:c.5224G>T
  • NM_001407726.1:c.5224G>T
  • NM_001407727.1:c.5224G>T
  • NM_001407728.1:c.5224G>T
  • NM_001407729.1:c.5224G>T
  • NM_001407730.1:c.5224G>T
  • NM_001407731.1:c.5224G>T
  • NM_001407732.1:c.5221G>T
  • NM_001407733.1:c.5221G>T
  • NM_001407734.1:c.5221G>T
  • NM_001407735.1:c.5221G>T
  • NM_001407736.1:c.5221G>T
  • NM_001407737.1:c.5221G>T
  • NM_001407738.1:c.5221G>T
  • NM_001407739.1:c.5221G>T
  • NM_001407740.1:c.5221G>T
  • NM_001407741.1:c.5221G>T
  • NM_001407742.1:c.5221G>T
  • NM_001407743.1:c.5221G>T
  • NM_001407744.1:c.5221G>T
  • NM_001407745.1:c.5221G>T
  • NM_001407746.1:c.5221G>T
  • NM_001407747.1:c.5221G>T
  • NM_001407748.1:c.5221G>T
  • NM_001407749.1:c.5221G>T
  • NM_001407750.1:c.5221G>T
  • NM_001407751.1:c.5221G>T
  • NM_001407752.1:c.5221G>T
  • NM_001407838.1:c.5218G>T
  • NM_001407839.1:c.5218G>T
  • NM_001407841.1:c.5218G>T
  • NM_001407842.1:c.5218G>T
  • NM_001407843.1:c.5218G>T
  • NM_001407844.1:c.5218G>T
  • NM_001407845.1:c.5218G>T
  • NM_001407846.1:c.5218G>T
  • NM_001407847.1:c.5218G>T
  • NM_001407848.1:c.5218G>T
  • NM_001407849.1:c.5218G>T
  • NM_001407850.1:c.5218G>T
  • NM_001407851.1:c.5218G>T
  • NM_001407852.1:c.5218G>T
  • NM_001407853.1:c.5218G>T
  • NM_001407862.1:c.5164G>T
  • NM_001407863.1:c.5161G>T
  • NM_001407874.1:c.5158G>T
  • NM_001407875.1:c.5158G>T
  • NM_001407879.1:c.5155G>T
  • NM_001407881.1:c.5155G>T
  • NM_001407882.1:c.5155G>T
  • NM_001407884.1:c.5155G>T
  • NM_001407885.1:c.5155G>T
  • NM_001407886.1:c.5155G>T
  • NM_001407887.1:c.5155G>T
  • NM_001407889.1:c.5155G>T
  • NM_001407894.1:c.5152G>T
  • NM_001407895.1:c.5152G>T
  • NM_001407896.1:c.5152G>T
  • NM_001407897.1:c.5152G>T
  • NM_001407898.1:c.5152G>T
  • NM_001407899.1:c.5152G>T
  • NM_001407900.1:c.5152G>T
  • NM_001407902.1:c.5152G>T
  • NM_001407904.1:c.5152G>T
  • NM_001407906.1:c.5152G>T
  • NM_001407907.1:c.5152G>T
  • NM_001407908.1:c.5152G>T
  • NM_001407909.1:c.5152G>T
  • NM_001407910.1:c.5152G>T
  • NM_001407915.1:c.5149G>T
  • NM_001407916.1:c.5149G>T
  • NM_001407917.1:c.5149G>T
  • NM_001407918.1:c.5149G>T
  • NM_001407920.1:c.5101G>T
  • NM_001407921.1:c.5101G>T
  • NM_001407922.1:c.5101G>T
  • NM_001407923.1:c.5101G>T
  • NM_001407924.1:c.5101G>T
  • NM_001407925.1:c.5101G>T
  • NM_001407926.1:c.5101G>T
  • NM_001407927.1:c.5098G>T
  • NM_001407928.1:c.5098G>T
  • NM_001407929.1:c.5098G>T
  • NM_001407930.1:c.5098G>T
  • NM_001407931.1:c.5098G>T
  • NM_001407932.1:c.5098G>T
  • NM_001407933.1:c.5098G>T
  • NM_001407934.1:c.5095G>T
  • NM_001407935.1:c.5095G>T
  • NM_001407936.1:c.5095G>T
  • NM_001407946.1:c.5032G>T
  • NM_001407947.1:c.5032G>T
  • NM_001407948.1:c.5032G>T
  • NM_001407949.1:c.5032G>T
  • NM_001407950.1:c.5029G>T
  • NM_001407951.1:c.5029G>T
  • NM_001407952.1:c.5029G>T
  • NM_001407953.1:c.5029G>T
  • NM_001407954.1:c.5029G>T
  • NM_001407955.1:c.5029G>T
  • NM_001407956.1:c.5026G>T
  • NM_001407957.1:c.5026G>T
  • NM_001407958.1:c.5026G>T
  • NM_001407959.1:c.4984G>T
  • NM_001407960.1:c.4981G>T
  • NM_001407962.1:c.4981G>T
  • NM_001407963.1:c.4978G>T
  • NM_001407964.1:c.4903G>T
  • NM_001407965.1:c.4858G>T
  • NM_001407966.1:c.4477G>T
  • NM_001407967.1:c.4474G>T
  • NM_001407968.1:c.2761G>T
  • NM_001407969.1:c.2758G>T
  • NM_001407970.1:c.2122G>T
  • NM_001407971.1:c.2122G>T
  • NM_001407972.1:c.2119G>T
  • NM_001407973.1:c.2056G>T
  • NM_001407974.1:c.2056G>T
  • NM_001407975.1:c.2056G>T
  • NM_001407976.1:c.2056G>T
  • NM_001407977.1:c.2056G>T
  • NM_001407978.1:c.2056G>T
  • NM_001407979.1:c.2053G>T
  • NM_001407980.1:c.2053G>T
  • NM_001407981.1:c.2053G>T
  • NM_001407982.1:c.2053G>T
  • NM_001407983.1:c.2053G>T
  • NM_001407984.1:c.2053G>T
  • NM_001407985.1:c.2053G>T
  • NM_001407986.1:c.2053G>T
  • NM_001407990.1:c.2053G>T
  • NM_001407991.1:c.2053G>T
  • NM_001407992.1:c.2053G>T
  • NM_001407993.1:c.2053G>T
  • NM_001408392.1:c.2050G>T
  • NM_001408396.1:c.2050G>T
  • NM_001408397.1:c.2050G>T
  • NM_001408398.1:c.2050G>T
  • NM_001408399.1:c.2050G>T
  • NM_001408400.1:c.2050G>T
  • NM_001408401.1:c.2050G>T
  • NM_001408402.1:c.2050G>T
  • NM_001408403.1:c.2050G>T
  • NM_001408404.1:c.2050G>T
  • NM_001408406.1:c.2047G>T
  • NM_001408407.1:c.2047G>T
  • NM_001408408.1:c.2047G>T
  • NM_001408409.1:c.2044G>T
  • NM_001408410.1:c.1981G>T
  • NM_001408411.1:c.1978G>T
  • NM_001408412.1:c.1975G>T
  • NM_001408413.1:c.1975G>T
  • NM_001408414.1:c.1975G>T
  • NM_001408415.1:c.1975G>T
  • NM_001408416.1:c.1975G>T
  • NM_001408418.1:c.1939G>T
  • NM_001408419.1:c.1939G>T
  • NM_001408420.1:c.1939G>T
  • NM_001408421.1:c.1936G>T
  • NM_001408422.1:c.1936G>T
  • NM_001408423.1:c.1936G>T
  • NM_001408424.1:c.1936G>T
  • NM_001408425.1:c.1933G>T
  • NM_001408426.1:c.1933G>T
  • NM_001408427.1:c.1933G>T
  • NM_001408428.1:c.1933G>T
  • NM_001408429.1:c.1933G>T
  • NM_001408430.1:c.1933G>T
  • NM_001408431.1:c.1933G>T
  • NM_001408432.1:c.1930G>T
  • NM_001408433.1:c.1930G>T
  • NM_001408434.1:c.1930G>T
  • NM_001408435.1:c.1930G>T
  • NM_001408436.1:c.1930G>T
  • NM_001408437.1:c.1930G>T
  • NM_001408438.1:c.1930G>T
  • NM_001408439.1:c.1930G>T
  • NM_001408440.1:c.1930G>T
  • NM_001408441.1:c.1930G>T
  • NM_001408442.1:c.1930G>T
  • NM_001408443.1:c.1930G>T
  • NM_001408444.1:c.1930G>T
  • NM_001408445.1:c.1927G>T
  • NM_001408446.1:c.1927G>T
  • NM_001408447.1:c.1927G>T
  • NM_001408448.1:c.1927G>T
  • NM_001408450.1:c.1927G>T
  • NM_001408451.1:c.1921G>T
  • NM_001408452.1:c.1915G>T
  • NM_001408453.1:c.1915G>T
  • NM_001408454.1:c.1915G>T
  • NM_001408455.1:c.1915G>T
  • NM_001408456.1:c.1915G>T
  • NM_001408457.1:c.1915G>T
  • NM_001408458.1:c.1912G>T
  • NM_001408459.1:c.1912G>T
  • NM_001408460.1:c.1912G>T
  • NM_001408461.1:c.1912G>T
  • NM_001408462.1:c.1912G>T
  • NM_001408463.1:c.1912G>T
  • NM_001408464.1:c.1912G>T
  • NM_001408465.1:c.1912G>T
  • NM_001408466.1:c.1912G>T
  • NM_001408467.1:c.1912G>T
  • NM_001408468.1:c.1909G>T
  • NM_001408469.1:c.1909G>T
  • NM_001408470.1:c.1909G>T
  • NM_001408474.1:c.1855G>T
  • NM_001408475.1:c.1852G>T
  • NM_001408476.1:c.1852G>T
  • NM_001408478.1:c.1846G>T
  • NM_001408479.1:c.1846G>T
  • NM_001408480.1:c.1846G>T
  • NM_001408481.1:c.1843G>T
  • NM_001408482.1:c.1843G>T
  • NM_001408483.1:c.1843G>T
  • NM_001408484.1:c.1843G>T
  • NM_001408485.1:c.1843G>T
  • NM_001408489.1:c.1843G>T
  • NM_001408490.1:c.1843G>T
  • NM_001408491.1:c.1843G>T
  • NM_001408492.1:c.1840G>T
  • NM_001408493.1:c.1840G>T
  • NM_001408494.1:c.1816G>T
  • NM_001408495.1:c.1810G>T
  • NM_001408496.1:c.1792G>T
  • NM_001408497.1:c.1792G>T
  • NM_001408498.1:c.1792G>T
  • NM_001408499.1:c.1792G>T
  • NM_001408500.1:c.1792G>T
  • NM_001408501.1:c.1792G>T
  • NM_001408502.1:c.1789G>T
  • NM_001408503.1:c.1789G>T
  • NM_001408504.1:c.1789G>T
  • NM_001408505.1:c.1786G>T
  • NM_001408506.1:c.1729G>T
  • NM_001408507.1:c.1726G>T
  • NM_001408508.1:c.1717G>T
  • NM_001408509.1:c.1714G>T
  • NM_001408510.1:c.1675G>T
  • NM_001408511.1:c.1672G>T
  • NM_001408512.1:c.1552G>T
  • NM_001408513.1:c.1525G>T
  • NM_001408514.1:c.1129G>T
  • NM_007294.4:c.5365G>TMANE SELECT
  • NM_007297.4:c.5224G>T
  • NM_007298.4:c.2053G>T
  • NM_007299.4:c.2021-1459G>T
  • NM_007300.4:c.5428G>T
  • NM_007304.2:c.2053G>T
  • NP_001394500.1:p.Ala1718Ser
  • NP_001394510.1:p.Ala1811Ser
  • NP_001394511.1:p.Ala1811Ser
  • NP_001394512.1:p.Ala1810Ser
  • NP_001394514.1:p.Ala1810Ser
  • NP_001394516.1:p.Ala1810Ser
  • NP_001394519.1:p.Ala1809Ser
  • NP_001394520.1:p.Ala1809Ser
  • NP_001394522.1:p.Ala1789Ser
  • NP_001394523.1:p.Ala1789Ser
  • NP_001394525.1:p.Ala1789Ser
  • NP_001394526.1:p.Ala1789Ser
  • NP_001394527.1:p.Ala1789Ser
  • NP_001394531.1:p.Ala1789Ser
  • NP_001394532.1:p.Ala1789Ser
  • NP_001394534.1:p.Ala1789Ser
  • NP_001394539.1:p.Ala1788Ser
  • NP_001394540.1:p.Ala1788Ser
  • NP_001394541.1:p.Ala1788Ser
  • NP_001394542.1:p.Ala1788Ser
  • NP_001394543.1:p.Ala1788Ser
  • NP_001394544.1:p.Ala1788Ser
  • NP_001394545.1:p.Ala1788Ser
  • NP_001394546.1:p.Ala1788Ser
  • NP_001394547.1:p.Ala1788Ser
  • NP_001394548.1:p.Ala1788Ser
  • NP_001394549.1:p.Ala1788Ser
  • NP_001394550.1:p.Ala1788Ser
  • NP_001394551.1:p.Ala1788Ser
  • NP_001394552.1:p.Ala1788Ser
  • NP_001394553.1:p.Ala1788Ser
  • NP_001394554.1:p.Ala1788Ser
  • NP_001394555.1:p.Ala1788Ser
  • NP_001394556.1:p.Ala1787Ser
  • NP_001394557.1:p.Ala1787Ser
  • NP_001394558.1:p.Ala1787Ser
  • NP_001394559.1:p.Ala1787Ser
  • NP_001394560.1:p.Ala1787Ser
  • NP_001394561.1:p.Ala1787Ser
  • NP_001394562.1:p.Ala1787Ser
  • NP_001394563.1:p.Ala1787Ser
  • NP_001394564.1:p.Ala1787Ser
  • NP_001394565.1:p.Ala1787Ser
  • NP_001394566.1:p.Ala1787Ser
  • NP_001394567.1:p.Ala1787Ser
  • NP_001394568.1:p.Ala1787Ser
  • NP_001394569.1:p.Ala1787Ser
  • NP_001394570.1:p.Ala1787Ser
  • NP_001394571.1:p.Ala1787Ser
  • NP_001394573.1:p.Ala1786Ser
  • NP_001394574.1:p.Ala1786Ser
  • NP_001394575.1:p.Ala1785Ser
  • NP_001394576.1:p.Ala1784Ser
  • NP_001394577.1:p.Ala1770Ser
  • NP_001394578.1:p.Ala1769Ser
  • NP_001394581.1:p.Ala1763Ser
  • NP_001394582.1:p.Ala1763Ser
  • NP_001394583.1:p.Ala1763Ser
  • NP_001394584.1:p.Ala1763Ser
  • NP_001394585.1:p.Ala1762Ser
  • NP_001394586.1:p.Ala1762Ser
  • NP_001394587.1:p.Ala1762Ser
  • NP_001394588.1:p.Ala1761Ser
  • NP_001394589.1:p.Ala1761Ser
  • NP_001394590.1:p.Ala1761Ser
  • NP_001394591.1:p.Ala1761Ser
  • NP_001394592.1:p.Ala1761Ser
  • NP_001394593.1:p.Ala1748Ser
  • NP_001394594.1:p.Ala1748Ser
  • NP_001394595.1:p.Ala1748Ser
  • NP_001394596.1:p.Ala1748Ser
  • NP_001394597.1:p.Ala1748Ser
  • NP_001394598.1:p.Ala1748Ser
  • NP_001394599.1:p.Ala1747Ser
  • NP_001394600.1:p.Ala1747Ser
  • NP_001394601.1:p.Ala1747Ser
  • NP_001394602.1:p.Ala1747Ser
  • NP_001394603.1:p.Ala1747Ser
  • NP_001394604.1:p.Ala1747Ser
  • NP_001394605.1:p.Ala1747Ser
  • NP_001394606.1:p.Ala1747Ser
  • NP_001394607.1:p.Ala1747Ser
  • NP_001394608.1:p.Ala1747Ser
  • NP_001394609.1:p.Ala1747Ser
  • NP_001394610.1:p.Ala1746Ser
  • NP_001394611.1:p.Ala1746Ser
  • NP_001394612.1:p.Ala1746Ser
  • NP_001394614.1:p.Ala1746Ser
  • NP_001394615.1:p.Ala1746Ser
  • NP_001394616.1:p.Ala1746Ser
  • NP_001394617.1:p.Ala1746Ser
  • NP_001394618.1:p.Ala1746Ser
  • NP_001394619.1:p.Ala1745Ser
  • NP_001394620.1:p.Ala1745Ser
  • NP_001394621.1:p.Ala1742Ser
  • NP_001394623.1:p.Ala1742Ser
  • NP_001394624.1:p.Ala1742Ser
  • NP_001394625.1:p.Ala1742Ser
  • NP_001394626.1:p.Ala1742Ser
  • NP_001394627.1:p.Ala1742Ser
  • NP_001394653.1:p.Ala1742Ser
  • NP_001394654.1:p.Ala1742Ser
  • NP_001394655.1:p.Ala1742Ser
  • NP_001394656.1:p.Ala1742Ser
  • NP_001394657.1:p.Ala1742Ser
  • NP_001394658.1:p.Ala1742Ser
  • NP_001394659.1:p.Ala1742Ser
  • NP_001394660.1:p.Ala1742Ser
  • NP_001394661.1:p.Ala1741Ser
  • NP_001394662.1:p.Ala1741Ser
  • NP_001394663.1:p.Ala1741Ser
  • NP_001394664.1:p.Ala1741Ser
  • NP_001394665.1:p.Ala1741Ser
  • NP_001394666.1:p.Ala1741Ser
  • NP_001394667.1:p.Ala1741Ser
  • NP_001394668.1:p.Ala1741Ser
  • NP_001394669.1:p.Ala1741Ser
  • NP_001394670.1:p.Ala1741Ser
  • NP_001394671.1:p.Ala1741Ser
  • NP_001394672.1:p.Ala1741Ser
  • NP_001394673.1:p.Ala1741Ser
  • NP_001394674.1:p.Ala1741Ser
  • NP_001394675.1:p.Ala1741Ser
  • NP_001394676.1:p.Ala1741Ser
  • NP_001394677.1:p.Ala1741Ser
  • NP_001394678.1:p.Ala1741Ser
  • NP_001394679.1:p.Ala1741Ser
  • NP_001394680.1:p.Ala1741Ser
  • NP_001394681.1:p.Ala1741Ser
  • NP_001394767.1:p.Ala1740Ser
  • NP_001394768.1:p.Ala1740Ser
  • NP_001394770.1:p.Ala1740Ser
  • NP_001394771.1:p.Ala1740Ser
  • NP_001394772.1:p.Ala1740Ser
  • NP_001394773.1:p.Ala1740Ser
  • NP_001394774.1:p.Ala1740Ser
  • NP_001394775.1:p.Ala1740Ser
  • NP_001394776.1:p.Ala1740Ser
  • NP_001394777.1:p.Ala1740Ser
  • NP_001394778.1:p.Ala1740Ser
  • NP_001394779.1:p.Ala1740Ser
  • NP_001394780.1:p.Ala1740Ser
  • NP_001394781.1:p.Ala1740Ser
  • NP_001394782.1:p.Ala1740Ser
  • NP_001394791.1:p.Ala1722Ser
  • NP_001394792.1:p.Ala1721Ser
  • NP_001394803.1:p.Ala1720Ser
  • NP_001394804.1:p.Ala1720Ser
  • NP_001394808.1:p.Ala1719Ser
  • NP_001394810.1:p.Ala1719Ser
  • NP_001394811.1:p.Ala1719Ser
  • NP_001394813.1:p.Ala1719Ser
  • NP_001394814.1:p.Ala1719Ser
  • NP_001394815.1:p.Ala1719Ser
  • NP_001394816.1:p.Ala1719Ser
  • NP_001394818.1:p.Ala1719Ser
  • NP_001394823.1:p.Ala1718Ser
  • NP_001394824.1:p.Ala1718Ser
  • NP_001394825.1:p.Ala1718Ser
  • NP_001394826.1:p.Ala1718Ser
  • NP_001394827.1:p.Ala1718Ser
  • NP_001394828.1:p.Ala1718Ser
  • NP_001394829.1:p.Ala1718Ser
  • NP_001394831.1:p.Ala1718Ser
  • NP_001394833.1:p.Ala1718Ser
  • NP_001394835.1:p.Ala1718Ser
  • NP_001394836.1:p.Ala1718Ser
  • NP_001394837.1:p.Ala1718Ser
  • NP_001394838.1:p.Ala1718Ser
  • NP_001394839.1:p.Ala1718Ser
  • NP_001394844.1:p.Ala1717Ser
  • NP_001394845.1:p.Ala1717Ser
  • NP_001394846.1:p.Ala1717Ser
  • NP_001394847.1:p.Ala1717Ser
  • NP_001394849.1:p.Ala1701Ser
  • NP_001394850.1:p.Ala1701Ser
  • NP_001394851.1:p.Ala1701Ser
  • NP_001394852.1:p.Ala1701Ser
  • NP_001394853.1:p.Ala1701Ser
  • NP_001394854.1:p.Ala1701Ser
  • NP_001394855.1:p.Ala1701Ser
  • NP_001394856.1:p.Ala1700Ser
  • NP_001394857.1:p.Ala1700Ser
  • NP_001394858.1:p.Ala1700Ser
  • NP_001394859.1:p.Ala1700Ser
  • NP_001394860.1:p.Ala1700Ser
  • NP_001394861.1:p.Ala1700Ser
  • NP_001394862.1:p.Ala1700Ser
  • NP_001394863.1:p.Ala1699Ser
  • NP_001394864.1:p.Ala1699Ser
  • NP_001394865.1:p.Ala1699Ser
  • NP_001394875.1:p.Ala1678Ser
  • NP_001394876.1:p.Ala1678Ser
  • NP_001394877.1:p.Ala1678Ser
  • NP_001394878.1:p.Ala1678Ser
  • NP_001394879.1:p.Ala1677Ser
  • NP_001394880.1:p.Ala1677Ser
  • NP_001394881.1:p.Ala1677Ser
  • NP_001394882.1:p.Ala1677Ser
  • NP_001394883.1:p.Ala1677Ser
  • NP_001394884.1:p.Ala1677Ser
  • NP_001394885.1:p.Ala1676Ser
  • NP_001394886.1:p.Ala1676Ser
  • NP_001394887.1:p.Ala1676Ser
  • NP_001394888.1:p.Ala1662Ser
  • NP_001394889.1:p.Ala1661Ser
  • NP_001394891.1:p.Ala1661Ser
  • NP_001394892.1:p.Ala1660Ser
  • NP_001394893.1:p.Ala1635Ser
  • NP_001394894.1:p.Ala1620Ser
  • NP_001394895.1:p.Ala1493Ser
  • NP_001394896.1:p.Ala1492Ser
  • NP_001394897.1:p.Ala921Ser
  • NP_001394898.1:p.Ala920Ser
  • NP_001394899.1:p.Ala708Ser
  • NP_001394900.1:p.Ala708Ser
  • NP_001394901.1:p.Ala707Ser
  • NP_001394902.1:p.Ala686Ser
  • NP_001394903.1:p.Ala686Ser
  • NP_001394904.1:p.Ala686Ser
  • NP_001394905.1:p.Ala686Ser
  • NP_001394906.1:p.Ala686Ser
  • NP_001394907.1:p.Ala686Ser
  • NP_001394908.1:p.Ala685Ser
  • NP_001394909.1:p.Ala685Ser
  • NP_001394910.1:p.Ala685Ser
  • NP_001394911.1:p.Ala685Ser
  • NP_001394912.1:p.Ala685Ser
  • NP_001394913.1:p.Ala685Ser
  • NP_001394914.1:p.Ala685Ser
  • NP_001394915.1:p.Ala685Ser
  • NP_001394919.1:p.Ala685Ser
  • NP_001394920.1:p.Ala685Ser
  • NP_001394921.1:p.Ala685Ser
  • NP_001394922.1:p.Ala685Ser
  • NP_001395321.1:p.Ala684Ser
  • NP_001395325.1:p.Ala684Ser
  • NP_001395326.1:p.Ala684Ser
  • NP_001395327.1:p.Ala684Ser
  • NP_001395328.1:p.Ala684Ser
  • NP_001395329.1:p.Ala684Ser
  • NP_001395330.1:p.Ala684Ser
  • NP_001395331.1:p.Ala684Ser
  • NP_001395332.1:p.Ala684Ser
  • NP_001395333.1:p.Ala684Ser
  • NP_001395335.1:p.Ala683Ser
  • NP_001395336.1:p.Ala683Ser
  • NP_001395337.1:p.Ala683Ser
  • NP_001395338.1:p.Ala682Ser
  • NP_001395339.1:p.Ala661Ser
  • NP_001395340.1:p.Ala660Ser
  • NP_001395341.1:p.Ala659Ser
  • NP_001395342.1:p.Ala659Ser
  • NP_001395343.1:p.Ala659Ser
  • NP_001395344.1:p.Ala659Ser
  • NP_001395345.1:p.Ala659Ser
  • NP_001395347.1:p.Ala647Ser
  • NP_001395348.1:p.Ala647Ser
  • NP_001395349.1:p.Ala647Ser
  • NP_001395350.1:p.Ala646Ser
  • NP_001395351.1:p.Ala646Ser
  • NP_001395352.1:p.Ala646Ser
  • NP_001395353.1:p.Ala646Ser
  • NP_001395354.1:p.Ala645Ser
  • NP_001395355.1:p.Ala645Ser
  • NP_001395356.1:p.Ala645Ser
  • NP_001395357.1:p.Ala645Ser
  • NP_001395358.1:p.Ala645Ser
  • NP_001395359.1:p.Ala645Ser
  • NP_001395360.1:p.Ala645Ser
  • NP_001395361.1:p.Ala644Ser
  • NP_001395362.1:p.Ala644Ser
  • NP_001395363.1:p.Ala644Ser
  • NP_001395364.1:p.Ala644Ser
  • NP_001395365.1:p.Ala644Ser
  • NP_001395366.1:p.Ala644Ser
  • NP_001395367.1:p.Ala644Ser
  • NP_001395368.1:p.Ala644Ser
  • NP_001395369.1:p.Ala644Ser
  • NP_001395370.1:p.Ala644Ser
  • NP_001395371.1:p.Ala644Ser
  • NP_001395372.1:p.Ala644Ser
  • NP_001395373.1:p.Ala644Ser
  • NP_001395374.1:p.Ala643Ser
  • NP_001395375.1:p.Ala643Ser
  • NP_001395376.1:p.Ala643Ser
  • NP_001395377.1:p.Ala643Ser
  • NP_001395379.1:p.Ala643Ser
  • NP_001395380.1:p.Ala641Ser
  • NP_001395381.1:p.Ala639Ser
  • NP_001395382.1:p.Ala639Ser
  • NP_001395383.1:p.Ala639Ser
  • NP_001395384.1:p.Ala639Ser
  • NP_001395385.1:p.Ala639Ser
  • NP_001395386.1:p.Ala639Ser
  • NP_001395387.1:p.Ala638Ser
  • NP_001395388.1:p.Ala638Ser
  • NP_001395389.1:p.Ala638Ser
  • NP_001395390.1:p.Ala638Ser
  • NP_001395391.1:p.Ala638Ser
  • NP_001395392.1:p.Ala638Ser
  • NP_001395393.1:p.Ala638Ser
  • NP_001395394.1:p.Ala638Ser
  • NP_001395395.1:p.Ala638Ser
  • NP_001395396.1:p.Ala638Ser
  • NP_001395397.1:p.Ala637Ser
  • NP_001395398.1:p.Ala637Ser
  • NP_001395399.1:p.Ala637Ser
  • NP_001395403.1:p.Ala619Ser
  • NP_001395404.1:p.Ala618Ser
  • NP_001395405.1:p.Ala618Ser
  • NP_001395407.1:p.Ala616Ser
  • NP_001395408.1:p.Ala616Ser
  • NP_001395409.1:p.Ala616Ser
  • NP_001395410.1:p.Ala615Ser
  • NP_001395411.1:p.Ala615Ser
  • NP_001395412.1:p.Ala615Ser
  • NP_001395413.1:p.Ala615Ser
  • NP_001395414.1:p.Ala615Ser
  • NP_001395418.1:p.Ala615Ser
  • NP_001395419.1:p.Ala615Ser
  • NP_001395420.1:p.Ala615Ser
  • NP_001395421.1:p.Ala614Ser
  • NP_001395422.1:p.Ala614Ser
  • NP_001395423.1:p.Ala606Ser
  • NP_001395424.1:p.Ala604Ser
  • NP_001395425.1:p.Ala598Ser
  • NP_001395426.1:p.Ala598Ser
  • NP_001395427.1:p.Ala598Ser
  • NP_001395428.1:p.Ala598Ser
  • NP_001395429.1:p.Ala598Ser
  • NP_001395430.1:p.Ala598Ser
  • NP_001395431.1:p.Ala597Ser
  • NP_001395432.1:p.Ala597Ser
  • NP_001395433.1:p.Ala597Ser
  • NP_001395434.1:p.Ala596Ser
  • NP_001395435.1:p.Ala577Ser
  • NP_001395436.1:p.Ala576Ser
  • NP_001395437.1:p.Ala573Ser
  • NP_001395438.1:p.Ala572Ser
  • NP_001395439.1:p.Ala559Ser
  • NP_001395440.1:p.Ala558Ser
  • NP_001395441.1:p.Ala518Ser
  • NP_001395442.1:p.Ala509Ser
  • NP_001395443.1:p.Ala377Ser
  • NP_009225.1:p.Ala1789Ser
  • NP_009225.1:p.Ala1789Ser
  • NP_009228.2:p.Ala1742Ser
  • NP_009229.2:p.Ala685Ser
  • NP_009229.2:p.Ala685Ser
  • NP_009231.2:p.Ala1810Ser
  • NP_009235.2:p.Ala685Ser
  • LRG_292t1:c.5365G>T
  • LRG_292:g.168822G>T
  • LRG_292p1:p.Ala1789Ser
  • NC_000017.10:g.41201179C>A
  • NM_007294.3:c.5365G>T
  • NM_007298.3:c.2053G>T
  • NR_027676.2:n.5542G>T
  • U14680.1:n.5484G>T
Protein change:
A1492S
Links:
dbSNP: rs80357078
NCBI 1000 Genomes Browser:
rs80357078
Molecular consequence:
  • NM_007299.4:c.2021-1459G>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.5431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.5431G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.5428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.5428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.5428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.5425G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.5425G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.5365G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.5365G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.5365G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.5365G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.5365G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.5365G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.5365G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.5365G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.5362G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.5359G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.5356G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.5356G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.5353G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.5350G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.5308G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.5305G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.5287G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.5287G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.5287G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.5287G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.5284G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.5284G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.5284G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.5281G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.5281G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.5281G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.5281G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.5281G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.5242G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.5242G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.5242G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.5242G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.5242G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.5242G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.5239G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.5236G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.5236G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.5236G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.5236G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.5236G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.5236G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.5236G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.5236G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.5233G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.5233G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.5221G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.5218G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.5164G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.5161G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.5158G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.5158G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.5155G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.5155G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.5155G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.5155G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.5155G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.5155G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.5155G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.5155G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.5152G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.5149G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.5149G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.5149G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.5149G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.5101G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.5101G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.5101G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.5101G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.5101G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.5101G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.5101G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.5098G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.5098G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.5098G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.5098G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.5098G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.5098G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.5098G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.5095G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.5095G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.5095G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.5032G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.5032G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.5032G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.5032G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.5029G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.5029G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.5029G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.5029G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.5029G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.5029G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.5026G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.5026G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.5026G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.4984G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.4981G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.4981G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.4978G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.4903G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.4858G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.4477G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.4474G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.2761G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.2758G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407970.1:c.2122G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407971.1:c.2122G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407972.1:c.2119G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407973.1:c.2056G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407974.1:c.2056G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407975.1:c.2056G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407976.1:c.2056G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407977.1:c.2056G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407978.1:c.2056G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407979.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407980.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407981.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407982.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407983.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407984.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407985.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407986.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407990.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407991.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407992.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407993.1:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408392.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408396.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408397.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408398.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408399.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408400.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408401.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408402.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408403.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408404.1:c.2050G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408406.1:c.2047G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408407.1:c.2047G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408408.1:c.2047G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408409.1:c.2044G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408410.1:c.1981G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408411.1:c.1978G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408412.1:c.1975G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408413.1:c.1975G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408414.1:c.1975G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408415.1:c.1975G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408416.1:c.1975G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408418.1:c.1939G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408419.1:c.1939G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408420.1:c.1939G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408421.1:c.1936G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408422.1:c.1936G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408423.1:c.1936G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408424.1:c.1936G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408425.1:c.1933G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408426.1:c.1933G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408427.1:c.1933G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408428.1:c.1933G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408429.1:c.1933G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408430.1:c.1933G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408431.1:c.1933G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408432.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408433.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408434.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408435.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408436.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408437.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408438.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408439.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408440.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408441.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408442.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408443.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408444.1:c.1930G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408445.1:c.1927G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408446.1:c.1927G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408447.1:c.1927G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408448.1:c.1927G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408450.1:c.1927G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408451.1:c.1921G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408452.1:c.1915G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408453.1:c.1915G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408454.1:c.1915G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408455.1:c.1915G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408456.1:c.1915G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408457.1:c.1915G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408458.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408459.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408460.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408461.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408462.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408463.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408464.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408465.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408466.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408467.1:c.1912G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408468.1:c.1909G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408469.1:c.1909G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408470.1:c.1909G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408474.1:c.1855G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408475.1:c.1852G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408476.1:c.1852G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408478.1:c.1846G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408479.1:c.1846G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408480.1:c.1846G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408481.1:c.1843G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408482.1:c.1843G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408483.1:c.1843G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408484.1:c.1843G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408485.1:c.1843G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408489.1:c.1843G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408490.1:c.1843G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408491.1:c.1843G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408492.1:c.1840G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408493.1:c.1840G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408494.1:c.1816G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408495.1:c.1810G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408496.1:c.1792G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408497.1:c.1792G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408498.1:c.1792G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408499.1:c.1792G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408500.1:c.1792G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408501.1:c.1792G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408502.1:c.1789G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408503.1:c.1789G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408504.1:c.1789G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408505.1:c.1786G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408506.1:c.1729G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408507.1:c.1726G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408508.1:c.1717G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408509.1:c.1714G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408510.1:c.1675G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408511.1:c.1672G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408512.1:c.1552G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408513.1:c.1525G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001408514.1:c.1129G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.5365G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.5224G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007298.4:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.5428G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007304.2:c.2053G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_027676.2:n.5542G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Functional consequence:
functionally_normal [Sequence Ontology: SO:0002219] - Comment(s)
Observations:
3

Condition(s)

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

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000145483Breast Cancer Information Core (BIC) (BRCA1)
no assertion criteria provided
Uncertain significance
(Dec 23, 2003)
germlineclinical testing

SCV000744585Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center - VKGL Data-share Consensus
criteria provided, single submitter

(ACGS Guidelines, 2013)
Likely benign
(Sep 21, 2015)
germlineclinical testing

Citation Link,

SCV000785154Counsyl
criteria provided, single submitter

(Counsyl Autosomal Dominant Disease Classification criteria (2015))
Uncertain significance
(May 9, 2017)
unknownclinical testing

PubMed (8)
[See all records that cite these PMIDs]

Counsyl_Autosomal_Dominant_Disease_Classification_criteria_(2015)_v1.pdf,

Citation Link,

SCV001243176Brotman Baty Institute, University of Washington
no classification provided
not providednot applicablein vitro

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

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical testing
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing
not providednot applicablenot applicablenot providednot providednot providednot providednot providedin vitro
Western Europeangermlineyes3not providednot providednot providednot providedclinical testing

Citations

PubMed

Probing structure-function relationships in missense variants in the carboxy-terminal region of BRCA1.

Carvalho RS, Abreu RB, Velkova A, Marsillac S, Rodarte RS, Suarez-Kurtz G, Iversen ES, Monteiro AN, Carvalho MA.

PLoS One. 2014;9(5):e97766. doi: 10.1371/journal.pone.0097766.

PubMed [citation]
PMID:
24845084
PMCID:
PMC4028255

Functional impact of missense variants in BRCA1 predicted by supervised learning.

Karchin R, Monteiro AN, Tavtigian SV, Carvalho MA, Sali A.

PLoS Comput Biol. 2007 Feb 16;3(2):e26. Epub 2006 Dec 28.

PubMed [citation]
PMID:
17305420
PMCID:
PMC1797820
See all PubMed Citations (9)

Details of each submission

From Breast Cancer Information Core (BIC) (BRCA1), SCV000145483.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1Western European3not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided3not providednot providednot provided

From Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center - VKGL Data-share Consensus, SCV000744585.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

From Counsyl, SCV000785154.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (8)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

From Brotman Baty Institute, University of Washington, SCV001243176.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedin vitro PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1not applicablenot applicablenot providednot providednot providednot providednot providednot providednot provided

Last Updated: Apr 15, 2024