NM_007294.4(BRCA1):c.3600G>C (p.Gln1200His) AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:: Benign/Likely benign (4 submissions)
Last evaluated:: Feb 5, 2024
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000112129.18

Allele description [Variation Report for NM_007294.4(BRCA1):c.3600G>C (p.Gln1200His)]

NM_007294.4(BRCA1):c.3600G>C (p.Gln1200His)

Genes:

BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]
LOC126862571:BRD4-independent group 4 enhancer GRCh37_chr17:41243136-41244335 [Gene]

Variant type:

single nucleotide variant

Cytogenetic location:

17q21.31

Genomic location:

Preferred name:

NM_007294.4(BRCA1):c.3600G>C (p.Gln1200His)

Other names:

p.Q1200H:CAG>CAC; NP_009225.1:p.Gln1200His

HGVS:

NC_000017.11:g.43091931C>G
NG_005905.2:g.126053G>C
NG_087068.1:g.913C>G
NM_001407571.1:c.3387G>C
NM_001407581.1:c.3600G>C
NM_001407582.1:c.3600G>C
NM_001407583.1:c.3600G>C
NM_001407585.1:c.3600G>C
NM_001407587.1:c.3597G>C
NM_001407590.1:c.3597G>C
NM_001407591.1:c.3597G>C
NM_001407593.1:c.3600G>C
NM_001407594.1:c.3600G>C
NM_001407596.1:c.3600G>C
NM_001407597.1:c.3600G>C
NM_001407598.1:c.3600G>C
NM_001407602.1:c.3600G>C
NM_001407603.1:c.3600G>C
NM_001407605.1:c.3600G>C
NM_001407610.1:c.3597G>C
NM_001407611.1:c.3597G>C
NM_001407612.1:c.3597G>C
NM_001407613.1:c.3597G>C
NM_001407614.1:c.3597G>C
NM_001407615.1:c.3597G>C
NM_001407616.1:c.3600G>C
NM_001407617.1:c.3600G>C
NM_001407618.1:c.3600G>C
NM_001407619.1:c.3600G>C
NM_001407620.1:c.3600G>C
NM_001407621.1:c.3600G>C
NM_001407622.1:c.3600G>C
NM_001407623.1:c.3600G>C
NM_001407624.1:c.3600G>C
NM_001407625.1:c.3600G>C
NM_001407626.1:c.3600G>C
NM_001407627.1:c.3597G>C
NM_001407628.1:c.3597G>C
NM_001407629.1:c.3597G>C
NM_001407630.1:c.3597G>C
NM_001407631.1:c.3597G>C
NM_001407632.1:c.3597G>C
NM_001407633.1:c.3597G>C
NM_001407634.1:c.3597G>C
NM_001407635.1:c.3597G>C
NM_001407636.1:c.3597G>C
NM_001407637.1:c.3597G>C
NM_001407638.1:c.3597G>C
NM_001407639.1:c.3600G>C
NM_001407640.1:c.3600G>C
NM_001407641.1:c.3600G>C
NM_001407642.1:c.3600G>C
NM_001407644.1:c.3597G>C
NM_001407645.1:c.3597G>C
NM_001407646.1:c.3591G>C
NM_001407647.1:c.3591G>C
NM_001407648.1:c.3477G>C
NM_001407649.1:c.3474G>C
NM_001407652.1:c.3600G>C
NM_001407653.1:c.3522G>C
NM_001407654.1:c.3522G>C
NM_001407655.1:c.3522G>C
NM_001407656.1:c.3522G>C
NM_001407657.1:c.3522G>C
NM_001407658.1:c.3522G>C
NM_001407659.1:c.3519G>C
NM_001407660.1:c.3519G>C
NM_001407661.1:c.3519G>C
NM_001407662.1:c.3519G>C
NM_001407663.1:c.3522G>C
NM_001407664.1:c.3477G>C
NM_001407665.1:c.3477G>C
NM_001407666.1:c.3477G>C
NM_001407667.1:c.3477G>C
NM_001407668.1:c.3477G>C
NM_001407669.1:c.3477G>C
NM_001407670.1:c.3474G>C
NM_001407671.1:c.3474G>C
NM_001407672.1:c.3474G>C
NM_001407673.1:c.3474G>C
NM_001407674.1:c.3477G>C
NM_001407675.1:c.3477G>C
NM_001407676.1:c.3477G>C
NM_001407677.1:c.3477G>C
NM_001407678.1:c.3477G>C
NM_001407679.1:c.3477G>C
NM_001407680.1:c.3477G>C
NM_001407681.1:c.3477G>C
NM_001407682.1:c.3477G>C
NM_001407683.1:c.3477G>C
NM_001407684.1:c.3600G>C
NM_001407685.1:c.3474G>C
NM_001407686.1:c.3474G>C
NM_001407687.1:c.3474G>C
NM_001407688.1:c.3474G>C
NM_001407689.1:c.3474G>C
NM_001407690.1:c.3474G>C
NM_001407691.1:c.3474G>C
NM_001407692.1:c.3459G>C
NM_001407694.1:c.3459G>C
NM_001407695.1:c.3459G>C
NM_001407696.1:c.3459G>C
NM_001407697.1:c.3459G>C
NM_001407698.1:c.3459G>C
NM_001407724.1:c.3459G>C
NM_001407725.1:c.3459G>C
NM_001407726.1:c.3459G>C
NM_001407727.1:c.3459G>C
NM_001407728.1:c.3459G>C
NM_001407729.1:c.3459G>C
NM_001407730.1:c.3459G>C
NM_001407731.1:c.3459G>C
NM_001407732.1:c.3459G>C
NM_001407733.1:c.3459G>C
NM_001407734.1:c.3459G>C
NM_001407735.1:c.3459G>C
NM_001407736.1:c.3459G>C
NM_001407737.1:c.3459G>C
NM_001407738.1:c.3459G>C
NM_001407739.1:c.3459G>C
NM_001407740.1:c.3456G>C
NM_001407741.1:c.3456G>C
NM_001407742.1:c.3456G>C
NM_001407743.1:c.3456G>C
NM_001407744.1:c.3456G>C
NM_001407745.1:c.3456G>C
NM_001407746.1:c.3456G>C
NM_001407747.1:c.3456G>C
NM_001407748.1:c.3456G>C
NM_001407749.1:c.3456G>C
NM_001407750.1:c.3459G>C
NM_001407751.1:c.3459G>C
NM_001407752.1:c.3459G>C
NM_001407838.1:c.3456G>C
NM_001407839.1:c.3456G>C
NM_001407841.1:c.3456G>C
NM_001407842.1:c.3456G>C
NM_001407843.1:c.3456G>C
NM_001407844.1:c.3456G>C
NM_001407845.1:c.3456G>C
NM_001407846.1:c.3456G>C
NM_001407847.1:c.3456G>C
NM_001407848.1:c.3456G>C
NM_001407849.1:c.3456G>C
NM_001407850.1:c.3459G>C
NM_001407851.1:c.3459G>C
NM_001407852.1:c.3459G>C
NM_001407853.1:c.3387G>C
NM_001407854.1:c.3600G>C
NM_001407858.1:c.3600G>C
NM_001407859.1:c.3600G>C
NM_001407860.1:c.3597G>C
NM_001407861.1:c.3597G>C
NM_001407862.1:c.3399G>C
NM_001407863.1:c.3477G>C
NM_001407874.1:c.3396G>C
NM_001407875.1:c.3396G>C
NM_001407879.1:c.3390G>C
NM_001407881.1:c.3390G>C
NM_001407882.1:c.3390G>C
NM_001407884.1:c.3390G>C
NM_001407885.1:c.3390G>C
NM_001407886.1:c.3390G>C
NM_001407887.1:c.3390G>C
NM_001407889.1:c.3390G>C
NM_001407894.1:c.3387G>C
NM_001407895.1:c.3387G>C
NM_001407896.1:c.3387G>C
NM_001407897.1:c.3387G>C
NM_001407898.1:c.3387G>C
NM_001407899.1:c.3387G>C
NM_001407900.1:c.3390G>C
NM_001407902.1:c.3390G>C
NM_001407904.1:c.3390G>C
NM_001407906.1:c.3390G>C
NM_001407907.1:c.3390G>C
NM_001407908.1:c.3390G>C
NM_001407909.1:c.3390G>C
NM_001407910.1:c.3390G>C
NM_001407915.1:c.3387G>C
NM_001407916.1:c.3387G>C
NM_001407917.1:c.3387G>C
NM_001407918.1:c.3387G>C
NM_001407919.1:c.3477G>C
NM_001407920.1:c.3336G>C
NM_001407921.1:c.3336G>C
NM_001407922.1:c.3336G>C
NM_001407923.1:c.3336G>C
NM_001407924.1:c.3336G>C
NM_001407925.1:c.3336G>C
NM_001407926.1:c.3336G>C
NM_001407927.1:c.3336G>C
NM_001407928.1:c.3336G>C
NM_001407929.1:c.3336G>C
NM_001407930.1:c.3333G>C
NM_001407931.1:c.3333G>C
NM_001407932.1:c.3333G>C
NM_001407933.1:c.3336G>C
NM_001407934.1:c.3333G>C
NM_001407935.1:c.3336G>C
NM_001407936.1:c.3333G>C
NM_001407937.1:c.3477G>C
NM_001407938.1:c.3477G>C
NM_001407939.1:c.3477G>C
NM_001407940.1:c.3474G>C
NM_001407941.1:c.3474G>C
NM_001407942.1:c.3459G>C
NM_001407943.1:c.3456G>C
NM_001407944.1:c.3459G>C
NM_001407945.1:c.3459G>C
NM_001407946.1:c.3267G>C
NM_001407947.1:c.3267G>C
NM_001407948.1:c.3267G>C
NM_001407949.1:c.3267G>C
NM_001407950.1:c.3267G>C
NM_001407951.1:c.3267G>C
NM_001407952.1:c.3267G>C
NM_001407953.1:c.3267G>C
NM_001407954.1:c.3264G>C
NM_001407955.1:c.3264G>C
NM_001407956.1:c.3264G>C
NM_001407957.1:c.3267G>C
NM_001407958.1:c.3264G>C
NM_001407959.1:c.3219G>C
NM_001407960.1:c.3219G>C
NM_001407962.1:c.3216G>C
NM_001407963.1:c.3219G>C
NM_001407964.1:c.3456G>C
NM_001407965.1:c.3096G>C
NM_001407966.1:c.2712G>C
NM_001407967.1:c.2712G>C
NM_001407968.1:c.996G>C
NM_001407969.1:c.996G>C
NM_001407970.1:c.788-899G>C
NM_001407971.1:c.788-899G>C
NM_001407972.1:c.785-899G>C
NM_001407973.1:c.788-899G>C
NM_001407974.1:c.788-899G>C
NM_001407975.1:c.788-899G>C
NM_001407976.1:c.788-899G>C
NM_001407977.1:c.788-899G>C
NM_001407978.1:c.788-899G>C
NM_001407979.1:c.788-899G>C
NM_001407980.1:c.788-899G>C
NM_001407981.1:c.788-899G>C
NM_001407982.1:c.788-899G>C
NM_001407983.1:c.788-899G>C
NM_001407984.1:c.785-899G>C
NM_001407985.1:c.785-899G>C
NM_001407986.1:c.785-899G>C
NM_001407990.1:c.788-899G>C
NM_001407991.1:c.785-899G>C
NM_001407992.1:c.785-899G>C
NM_001407993.1:c.788-899G>C
NM_001408392.1:c.785-899G>C
NM_001408396.1:c.785-899G>C
NM_001408397.1:c.785-899G>C
NM_001408398.1:c.785-899G>C
NM_001408399.1:c.785-899G>C
NM_001408400.1:c.785-899G>C
NM_001408401.1:c.785-899G>C
NM_001408402.1:c.785-899G>C
NM_001408403.1:c.788-899G>C
NM_001408404.1:c.788-899G>C
NM_001408406.1:c.791-908G>C
NM_001408407.1:c.785-899G>C
NM_001408408.1:c.779-899G>C
NM_001408409.1:c.710-899G>C
NM_001408410.1:c.647-899G>C
NM_001408411.1:c.710-899G>C
NM_001408412.1:c.710-899G>C
NM_001408413.1:c.707-899G>C
NM_001408414.1:c.710-899G>C
NM_001408415.1:c.710-899G>C
NM_001408416.1:c.707-899G>C
NM_001408418.1:c.671-899G>C
NM_001408419.1:c.671-899G>C
NM_001408420.1:c.671-899G>C
NM_001408421.1:c.668-899G>C
NM_001408422.1:c.671-899G>C
NM_001408423.1:c.671-899G>C
NM_001408424.1:c.668-899G>C
NM_001408425.1:c.665-899G>C
NM_001408426.1:c.665-899G>C
NM_001408427.1:c.665-899G>C
NM_001408428.1:c.665-899G>C
NM_001408429.1:c.665-899G>C
NM_001408430.1:c.665-899G>C
NM_001408431.1:c.668-899G>C
NM_001408432.1:c.662-899G>C
NM_001408433.1:c.662-899G>C
NM_001408434.1:c.662-899G>C
NM_001408435.1:c.662-899G>C
NM_001408436.1:c.665-899G>C
NM_001408437.1:c.665-899G>C
NM_001408438.1:c.665-899G>C
NM_001408439.1:c.665-899G>C
NM_001408440.1:c.665-899G>C
NM_001408441.1:c.665-899G>C
NM_001408442.1:c.665-899G>C
NM_001408443.1:c.665-899G>C
NM_001408444.1:c.665-899G>C
NM_001408445.1:c.662-899G>C
NM_001408446.1:c.662-899G>C
NM_001408447.1:c.662-899G>C
NM_001408448.1:c.662-899G>C
NM_001408450.1:c.662-899G>C
NM_001408451.1:c.653-899G>C
NM_001408452.1:c.647-899G>C
NM_001408453.1:c.647-899G>C
NM_001408454.1:c.647-899G>C
NM_001408455.1:c.647-899G>C
NM_001408456.1:c.647-899G>C
NM_001408457.1:c.647-899G>C
NM_001408458.1:c.647-899G>C
NM_001408459.1:c.647-899G>C
NM_001408460.1:c.647-899G>C
NM_001408461.1:c.647-899G>C
NM_001408462.1:c.644-899G>C
NM_001408463.1:c.644-899G>C
NM_001408464.1:c.644-899G>C
NM_001408465.1:c.644-899G>C
NM_001408466.1:c.647-899G>C
NM_001408467.1:c.647-899G>C
NM_001408468.1:c.644-899G>C
NM_001408469.1:c.647-899G>C
NM_001408470.1:c.644-899G>C
NM_001408472.1:c.788-899G>C
NM_001408473.1:c.785-899G>C
NM_001408474.1:c.587-899G>C
NM_001408475.1:c.584-899G>C
NM_001408476.1:c.587-899G>C
NM_001408478.1:c.578-899G>C
NM_001408479.1:c.578-899G>C
NM_001408480.1:c.578-899G>C
NM_001408481.1:c.578-899G>C
NM_001408482.1:c.578-899G>C
NM_001408483.1:c.578-899G>C
NM_001408484.1:c.578-899G>C
NM_001408485.1:c.578-899G>C
NM_001408489.1:c.578-899G>C
NM_001408490.1:c.575-899G>C
NM_001408491.1:c.575-899G>C
NM_001408492.1:c.578-899G>C
NM_001408493.1:c.575-899G>C
NM_001408494.1:c.548-899G>C
NM_001408495.1:c.545-899G>C
NM_001408496.1:c.524-899G>C
NM_001408497.1:c.524-899G>C
NM_001408498.1:c.524-899G>C
NM_001408499.1:c.524-899G>C
NM_001408500.1:c.524-899G>C
NM_001408501.1:c.524-899G>C
NM_001408502.1:c.455-899G>C
NM_001408503.1:c.521-899G>C
NM_001408504.1:c.521-899G>C
NM_001408505.1:c.521-899G>C
NM_001408506.1:c.461-899G>C
NM_001408507.1:c.461-899G>C
NM_001408508.1:c.452-899G>C
NM_001408509.1:c.452-899G>C
NM_001408510.1:c.407-899G>C
NM_001408511.1:c.404-899G>C
NM_001408512.1:c.284-899G>C
NM_001408513.1:c.578-899G>C
NM_001408514.1:c.578-899G>C
NM_007294.4:c.3600G>CMANE SELECT
NM_007297.4:c.3459G>C
NM_007298.4:c.788-899G>C
NM_007299.4:c.788-899G>C
NM_007300.4:c.3600G>C
NP_001394500.1:p.Gln1129His
NP_001394510.1:p.Gln1200His
NP_001394511.1:p.Gln1200His
NP_001394512.1:p.Gln1200His
NP_001394514.1:p.Gln1200His
NP_001394516.1:p.Gln1199His
NP_001394519.1:p.Gln1199His
NP_001394520.1:p.Gln1199His
NP_001394522.1:p.Gln1200His
NP_001394523.1:p.Gln1200His
NP_001394525.1:p.Gln1200His
NP_001394526.1:p.Gln1200His
NP_001394527.1:p.Gln1200His
NP_001394531.1:p.Gln1200His
NP_001394532.1:p.Gln1200His
NP_001394534.1:p.Gln1200His
NP_001394539.1:p.Gln1199His
NP_001394540.1:p.Gln1199His
NP_001394541.1:p.Gln1199His
NP_001394542.1:p.Gln1199His
NP_001394543.1:p.Gln1199His
NP_001394544.1:p.Gln1199His
NP_001394545.1:p.Gln1200His
NP_001394546.1:p.Gln1200His
NP_001394547.1:p.Gln1200His
NP_001394548.1:p.Gln1200His
NP_001394549.1:p.Gln1200His
NP_001394550.1:p.Gln1200His
NP_001394551.1:p.Gln1200His
NP_001394552.1:p.Gln1200His
NP_001394553.1:p.Gln1200His
NP_001394554.1:p.Gln1200His
NP_001394555.1:p.Gln1200His
NP_001394556.1:p.Gln1199His
NP_001394557.1:p.Gln1199His
NP_001394558.1:p.Gln1199His
NP_001394559.1:p.Gln1199His
NP_001394560.1:p.Gln1199His
NP_001394561.1:p.Gln1199His
NP_001394562.1:p.Gln1199His
NP_001394563.1:p.Gln1199His
NP_001394564.1:p.Gln1199His
NP_001394565.1:p.Gln1199His
NP_001394566.1:p.Gln1199His
NP_001394567.1:p.Gln1199His
NP_001394568.1:p.Gln1200His
NP_001394569.1:p.Gln1200His
NP_001394570.1:p.Gln1200His
NP_001394571.1:p.Gln1200His
NP_001394573.1:p.Gln1199His
NP_001394574.1:p.Gln1199His
NP_001394575.1:p.Gln1197His
NP_001394576.1:p.Gln1197His
NP_001394577.1:p.Gln1159His
NP_001394578.1:p.Gln1158His
NP_001394581.1:p.Gln1200His
NP_001394582.1:p.Gln1174His
NP_001394583.1:p.Gln1174His
NP_001394584.1:p.Gln1174His
NP_001394585.1:p.Gln1174His
NP_001394586.1:p.Gln1174His
NP_001394587.1:p.Gln1174His
NP_001394588.1:p.Gln1173His
NP_001394589.1:p.Gln1173His
NP_001394590.1:p.Gln1173His
NP_001394591.1:p.Gln1173His
NP_001394592.1:p.Gln1174His
NP_001394593.1:p.Gln1159His
NP_001394594.1:p.Gln1159His
NP_001394595.1:p.Gln1159His
NP_001394596.1:p.Gln1159His
NP_001394597.1:p.Gln1159His
NP_001394598.1:p.Gln1159His
NP_001394599.1:p.Gln1158His
NP_001394600.1:p.Gln1158His
NP_001394601.1:p.Gln1158His
NP_001394602.1:p.Gln1158His
NP_001394603.1:p.Gln1159His
NP_001394604.1:p.Gln1159His
NP_001394605.1:p.Gln1159His
NP_001394606.1:p.Gln1159His
NP_001394607.1:p.Gln1159His
NP_001394608.1:p.Gln1159His
NP_001394609.1:p.Gln1159His
NP_001394610.1:p.Gln1159His
NP_001394611.1:p.Gln1159His
NP_001394612.1:p.Gln1159His
NP_001394613.1:p.Gln1200His
NP_001394614.1:p.Gln1158His
NP_001394615.1:p.Gln1158His
NP_001394616.1:p.Gln1158His
NP_001394617.1:p.Gln1158His
NP_001394618.1:p.Gln1158His
NP_001394619.1:p.Gln1158His
NP_001394620.1:p.Gln1158His
NP_001394621.1:p.Gln1153His
NP_001394623.1:p.Gln1153His
NP_001394624.1:p.Gln1153His
NP_001394625.1:p.Gln1153His
NP_001394626.1:p.Gln1153His
NP_001394627.1:p.Gln1153His
NP_001394653.1:p.Gln1153His
NP_001394654.1:p.Gln1153His
NP_001394655.1:p.Gln1153His
NP_001394656.1:p.Gln1153His
NP_001394657.1:p.Gln1153His
NP_001394658.1:p.Gln1153His
NP_001394659.1:p.Gln1153His
NP_001394660.1:p.Gln1153His
NP_001394661.1:p.Gln1153His
NP_001394662.1:p.Gln1153His
NP_001394663.1:p.Gln1153His
NP_001394664.1:p.Gln1153His
NP_001394665.1:p.Gln1153His
NP_001394666.1:p.Gln1153His
NP_001394667.1:p.Gln1153His
NP_001394668.1:p.Gln1153His
NP_001394669.1:p.Gln1152His
NP_001394670.1:p.Gln1152His
NP_001394671.1:p.Gln1152His
NP_001394672.1:p.Gln1152His
NP_001394673.1:p.Gln1152His
NP_001394674.1:p.Gln1152His
NP_001394675.1:p.Gln1152His
NP_001394676.1:p.Gln1152His
NP_001394677.1:p.Gln1152His
NP_001394678.1:p.Gln1152His
NP_001394679.1:p.Gln1153His
NP_001394680.1:p.Gln1153His
NP_001394681.1:p.Gln1153His
NP_001394767.1:p.Gln1152His
NP_001394768.1:p.Gln1152His
NP_001394770.1:p.Gln1152His
NP_001394771.1:p.Gln1152His
NP_001394772.1:p.Gln1152His
NP_001394773.1:p.Gln1152His
NP_001394774.1:p.Gln1152His
NP_001394775.1:p.Gln1152His
NP_001394776.1:p.Gln1152His
NP_001394777.1:p.Gln1152His
NP_001394778.1:p.Gln1152His
NP_001394779.1:p.Gln1153His
NP_001394780.1:p.Gln1153His
NP_001394781.1:p.Gln1153His
NP_001394782.1:p.Gln1129His
NP_001394783.1:p.Gln1200His
NP_001394787.1:p.Gln1200His
NP_001394788.1:p.Gln1200His
NP_001394789.1:p.Gln1199His
NP_001394790.1:p.Gln1199His
NP_001394791.1:p.Gln1133His
NP_001394792.1:p.Gln1159His
NP_001394803.1:p.Gln1132His
NP_001394804.1:p.Gln1132His
NP_001394808.1:p.Gln1130His
NP_001394810.1:p.Gln1130His
NP_001394811.1:p.Gln1130His
NP_001394813.1:p.Gln1130His
NP_001394814.1:p.Gln1130His
NP_001394815.1:p.Gln1130His
NP_001394816.1:p.Gln1130His
NP_001394818.1:p.Gln1130His
NP_001394823.1:p.Gln1129His
NP_001394824.1:p.Gln1129His
NP_001394825.1:p.Gln1129His
NP_001394826.1:p.Gln1129His
NP_001394827.1:p.Gln1129His
NP_001394828.1:p.Gln1129His
NP_001394829.1:p.Gln1130His
NP_001394831.1:p.Gln1130His
NP_001394833.1:p.Gln1130His
NP_001394835.1:p.Gln1130His
NP_001394836.1:p.Gln1130His
NP_001394837.1:p.Gln1130His
NP_001394838.1:p.Gln1130His
NP_001394839.1:p.Gln1130His
NP_001394844.1:p.Gln1129His
NP_001394845.1:p.Gln1129His
NP_001394846.1:p.Gln1129His
NP_001394847.1:p.Gln1129His
NP_001394848.1:p.Gln1159His
NP_001394849.1:p.Gln1112His
NP_001394850.1:p.Gln1112His
NP_001394851.1:p.Gln1112His
NP_001394852.1:p.Gln1112His
NP_001394853.1:p.Gln1112His
NP_001394854.1:p.Gln1112His
NP_001394855.1:p.Gln1112His
NP_001394856.1:p.Gln1112His
NP_001394857.1:p.Gln1112His
NP_001394858.1:p.Gln1112His
NP_001394859.1:p.Gln1111His
NP_001394860.1:p.Gln1111His
NP_001394861.1:p.Gln1111His
NP_001394862.1:p.Gln1112His
NP_001394863.1:p.Gln1111His
NP_001394864.1:p.Gln1112His
NP_001394865.1:p.Gln1111His
NP_001394866.1:p.Gln1159His
NP_001394867.1:p.Gln1159His
NP_001394868.1:p.Gln1159His
NP_001394869.1:p.Gln1158His
NP_001394870.1:p.Gln1158His
NP_001394871.1:p.Gln1153His
NP_001394872.1:p.Gln1152His
NP_001394873.1:p.Gln1153His
NP_001394874.1:p.Gln1153His
NP_001394875.1:p.Gln1089His
NP_001394876.1:p.Gln1089His
NP_001394877.1:p.Gln1089His
NP_001394878.1:p.Gln1089His
NP_001394879.1:p.Gln1089His
NP_001394880.1:p.Gln1089His
NP_001394881.1:p.Gln1089His
NP_001394882.1:p.Gln1089His
NP_001394883.1:p.Gln1088His
NP_001394884.1:p.Gln1088His
NP_001394885.1:p.Gln1088His
NP_001394886.1:p.Gln1089His
NP_001394887.1:p.Gln1088His
NP_001394888.1:p.Gln1073His
NP_001394889.1:p.Gln1073His
NP_001394891.1:p.Gln1072His
NP_001394892.1:p.Gln1073His
NP_001394893.1:p.Gln1152His
NP_001394894.1:p.Gln1032His
NP_001394895.1:p.Gln904His
NP_001394896.1:p.Gln904His
NP_001394897.1:p.Gln332His
NP_001394898.1:p.Gln332His
NP_009225.1:p.Gln1200His
NP_009225.1:p.Gln1200His
NP_009228.2:p.Gln1153His
NP_009231.2:p.Gln1200His
LRG_292t1:c.3600G>C
LRG_292:g.126053G>C
LRG_292p1:p.Gln1200His
NC_000017.10:g.41243948C>G
NM_007294.3:c.3600G>C
NM_007294.4:c.3600G>C
NM_007299.3:c.788-899G>C
NR_027676.1:n.3736G>C
P38398:p.Gln1200His
U14680.1:n.3719G>C
p.Q1200H

Protein change:

Q1032H

Links:

UniProtKB: P38398#VAR_020691; dbSNP: rs56214134

NCBI 1000 Genomes Browser:

rs56214134

Molecular consequence:

NM_001407970.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407971.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407972.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407973.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407974.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407975.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407976.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407977.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407978.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407979.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407980.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407981.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407982.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407983.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407984.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407985.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407986.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407990.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407991.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407992.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407993.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408392.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408396.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408397.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408398.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408399.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408400.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408401.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408402.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408403.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408404.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408406.1:c.791-908G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408407.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408408.1:c.779-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408409.1:c.710-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408410.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408411.1:c.710-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408412.1:c.710-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408413.1:c.707-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408414.1:c.710-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408415.1:c.710-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408416.1:c.707-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408418.1:c.671-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408419.1:c.671-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408420.1:c.671-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408421.1:c.668-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408422.1:c.671-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408423.1:c.671-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408424.1:c.668-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408425.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408426.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408427.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408428.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408429.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408430.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408431.1:c.668-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408432.1:c.662-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408433.1:c.662-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408434.1:c.662-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408435.1:c.662-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408436.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408437.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408438.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408439.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408440.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408441.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408442.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408443.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408444.1:c.665-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408445.1:c.662-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408446.1:c.662-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408447.1:c.662-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408448.1:c.662-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408450.1:c.662-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408451.1:c.653-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408452.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408453.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408454.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408455.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408456.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408457.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408458.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408459.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408460.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408461.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408462.1:c.644-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408463.1:c.644-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408464.1:c.644-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408465.1:c.644-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408466.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408467.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408468.1:c.644-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408469.1:c.647-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408470.1:c.644-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408472.1:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408473.1:c.785-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408474.1:c.587-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408475.1:c.584-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408476.1:c.587-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408478.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408479.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408480.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408481.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408482.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408483.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408484.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408485.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408489.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408490.1:c.575-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408491.1:c.575-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408492.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408493.1:c.575-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408494.1:c.548-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408495.1:c.545-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408496.1:c.524-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408497.1:c.524-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408498.1:c.524-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408499.1:c.524-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408500.1:c.524-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408501.1:c.524-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408502.1:c.455-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408503.1:c.521-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408504.1:c.521-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408505.1:c.521-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408506.1:c.461-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408507.1:c.461-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408508.1:c.452-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408509.1:c.452-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408510.1:c.407-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408511.1:c.404-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408512.1:c.284-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408513.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001408514.1:c.578-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_007298.4:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_007299.4:c.788-899G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001407571.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407581.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407582.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407583.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407585.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407587.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407590.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407591.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407593.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407594.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407596.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407597.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407598.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407602.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407603.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407605.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407610.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407611.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407612.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407613.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407614.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407615.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407616.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407617.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407618.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407619.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407620.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407621.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407622.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407623.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407624.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407625.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407626.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407627.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407628.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407629.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407630.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407631.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407632.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407633.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407634.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407635.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407636.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407637.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407638.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407639.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407640.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407641.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407642.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407644.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407645.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407646.1:c.3591G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407647.1:c.3591G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407648.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407649.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407652.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407653.1:c.3522G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407654.1:c.3522G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407655.1:c.3522G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407656.1:c.3522G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407657.1:c.3522G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407658.1:c.3522G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407659.1:c.3519G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407660.1:c.3519G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407661.1:c.3519G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407662.1:c.3519G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407663.1:c.3522G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407664.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407665.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407666.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407667.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407668.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407669.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407670.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407671.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407672.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407673.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407674.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407675.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407676.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407677.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407678.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407679.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407680.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407681.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407682.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407683.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407684.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407685.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407686.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407687.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407688.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407689.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407690.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407691.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407692.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407694.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407695.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407696.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407697.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407698.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407724.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407725.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407726.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407727.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407728.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407729.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407730.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407731.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407732.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407733.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407734.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407735.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407736.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407737.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407738.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407739.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407740.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407741.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407742.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407743.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407744.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407745.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407746.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407747.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407748.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407749.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407750.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407751.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407752.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407838.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407839.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407841.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407842.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407843.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407844.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407845.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407846.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407847.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407848.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407849.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407850.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407851.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407852.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407853.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407854.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407858.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407859.1:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407860.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407861.1:c.3597G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407862.1:c.3399G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407863.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407874.1:c.3396G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407875.1:c.3396G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407879.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407881.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407882.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407884.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407885.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407886.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407887.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407889.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407894.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407895.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407896.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407897.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407898.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407899.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407900.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407902.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407904.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407906.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407907.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407908.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407909.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407910.1:c.3390G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407915.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407916.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407917.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407918.1:c.3387G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407919.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407920.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407921.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407922.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407923.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407924.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407925.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407926.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407927.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407928.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407929.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407930.1:c.3333G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407931.1:c.3333G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407932.1:c.3333G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407933.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407934.1:c.3333G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407935.1:c.3336G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407936.1:c.3333G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407937.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407938.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407939.1:c.3477G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407940.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407941.1:c.3474G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407942.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407943.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407944.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407945.1:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407946.1:c.3267G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407947.1:c.3267G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407948.1:c.3267G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407949.1:c.3267G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407950.1:c.3267G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407951.1:c.3267G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407952.1:c.3267G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407953.1:c.3267G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407954.1:c.3264G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407955.1:c.3264G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407956.1:c.3264G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407957.1:c.3267G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407958.1:c.3264G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407959.1:c.3219G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407960.1:c.3219G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407962.1:c.3216G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407963.1:c.3219G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407964.1:c.3456G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407965.1:c.3096G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407966.1:c.2712G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407967.1:c.2712G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407968.1:c.996G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001407969.1:c.996G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_007294.4:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_007297.4:c.3459G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_007300.4:c.3600G>C - missense variant - [Sequence Ontology: SO:0001583]

Observations:

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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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000144802	Breast Cancer Information Core (BIC) (BRCA1)	no assertion criteria provided	Benign (May 29, 2002)	germline	clinical testing
SCV000195923	Michigan Medical Genetics Laboratories, University of Michigan	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Nov 3, 2014)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV000220665	Counsyl	criteria provided, single submitter (Counsyl Autosomal Dominant Disease Classification criteria (2015))	Likely benign (Sep 3, 2014)	unknown	literature only	PubMed (6) [See all records that cite these PMIDs] 18284688, 17279547, 15726418, 22034289, 20104584, 16267036 Counsyl Autosomal Dominant Disease Classification criteria (2015), Citation Link,
SCV004817781	All of Us Research Program, National Institutes of Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely Benign (Feb 5, 2024)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

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Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	3	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	66	not provided	not provided	108544	not provided	clinical testing
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	literature only
African	germline	yes	11	not provided	not provided	not provided	not provided	clinical testing
African American, Central/Eastern European	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing
Native American	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing
Western European, Jamaican (Africian), Scottish	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Evaluation of unclassified variants in the breast cancer susceptibility genes BRCA1 and BRCA2 using five methods: results from a population-based study of young breast cancer patients.

Lee E, McKean-Cowdin R, Ma H, Chen Z, Van Den Berg D, Henderson BE, Bernstein L, Ursin G.

Breast Cancer Res. 2008;10(1):R19. doi: 10.1186/bcr1865. Epub 2008 Feb 19.

PubMed [citation]

PMID:: 18284688
PMCID:: PMC2374975

Classification of missense variants of unknown significance in BRCA1 based on clinical and tumor information.

Osorio A, Milne RL, Honrado E, Barroso A, Diez O, Salazar R, de la Hoya M, Vega A, Benítez J.

Hum Mutat. 2007 May;28(5):477-85.

PubMed [citation]

PMID:: 17279547

See all PubMed Citations (7)

Details of each submission

From Breast Cancer Information Core (BIC) (BRCA1), SCV000144802.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	1	not provided	not provided	clinical testing	not provided
2	not provided	1	not provided	not provided	clinical testing	not provided
3	not provided	1	not provided	not provided	clinical testing	not provided
4	African	11	not provided	not provided	clinical testing	not provided
5	African American, Central/Eastern European	1	not provided	not provided	clinical testing	not provided
6	Native American	1	not provided	not provided	clinical testing	not provided
7	Western European, Jamaican (Africian), Scottish	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		1	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		11	not provided	not provided	not provided
5	germline	yes	not provided	not provided	not provided		1	not provided	not provided	not provided
6	germline	yes	not provided	not provided	not provided		1	not provided	not provided	not provided
7	germline	yes	not provided	not provided	not provided		1	not provided	not provided	not provided

From Michigan Medical Genetics Laboratories, University of Michigan, SCV000195923.1

#	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	Blood	not provided		not provided	not provided	not provided	not provided

From Counsyl, SCV000220665.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	literature only	PubMed (6)

#	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 All of Us Research Program, National Institutes of Health, SCV004817781.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	66	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	unknown	108544	not provided	not provided		66	not provided	not provided	not provided

Last Updated: Sep 8, 2024

ClinVar

Relating variation to medicine