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NM_007294.4(BRCA1):c.3260G>C (p.Gly1087Ala) AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Mar 4, 2023
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV000112040.6

Allele description [Variation Report for NM_007294.4(BRCA1):c.3260G>C (p.Gly1087Ala)]

NM_007294.4(BRCA1):c.3260G>C (p.Gly1087Ala)

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.3260G>C (p.Gly1087Ala)
Other names:
p.G1087A:GGG>GCG
HGVS:
  • NC_000017.11:g.43092271C>G
  • NG_005905.2:g.125713G>C
  • NG_087068.1:g.1253C>G
  • NM_001407571.1:c.3047G>C
  • NM_001407581.1:c.3260G>C
  • NM_001407582.1:c.3260G>C
  • NM_001407583.1:c.3260G>C
  • NM_001407585.1:c.3260G>C
  • NM_001407587.1:c.3257G>C
  • NM_001407590.1:c.3257G>C
  • NM_001407591.1:c.3257G>C
  • NM_001407593.1:c.3260G>C
  • NM_001407594.1:c.3260G>C
  • NM_001407596.1:c.3260G>C
  • NM_001407597.1:c.3260G>C
  • NM_001407598.1:c.3260G>C
  • NM_001407602.1:c.3260G>C
  • NM_001407603.1:c.3260G>C
  • NM_001407605.1:c.3260G>C
  • NM_001407610.1:c.3257G>C
  • NM_001407611.1:c.3257G>C
  • NM_001407612.1:c.3257G>C
  • NM_001407613.1:c.3257G>C
  • NM_001407614.1:c.3257G>C
  • NM_001407615.1:c.3257G>C
  • NM_001407616.1:c.3260G>C
  • NM_001407617.1:c.3260G>C
  • NM_001407618.1:c.3260G>C
  • NM_001407619.1:c.3260G>C
  • NM_001407620.1:c.3260G>C
  • NM_001407621.1:c.3260G>C
  • NM_001407622.1:c.3260G>C
  • NM_001407623.1:c.3260G>C
  • NM_001407624.1:c.3260G>C
  • NM_001407625.1:c.3260G>C
  • NM_001407626.1:c.3260G>C
  • NM_001407627.1:c.3257G>C
  • NM_001407628.1:c.3257G>C
  • NM_001407629.1:c.3257G>C
  • NM_001407630.1:c.3257G>C
  • NM_001407631.1:c.3257G>C
  • NM_001407632.1:c.3257G>C
  • NM_001407633.1:c.3257G>C
  • NM_001407634.1:c.3257G>C
  • NM_001407635.1:c.3257G>C
  • NM_001407636.1:c.3257G>C
  • NM_001407637.1:c.3257G>C
  • NM_001407638.1:c.3257G>C
  • NM_001407639.1:c.3260G>C
  • NM_001407640.1:c.3260G>C
  • NM_001407641.1:c.3260G>C
  • NM_001407642.1:c.3260G>C
  • NM_001407644.1:c.3257G>C
  • NM_001407645.1:c.3257G>C
  • NM_001407646.1:c.3251G>C
  • NM_001407647.1:c.3251G>C
  • NM_001407648.1:c.3137G>C
  • NM_001407649.1:c.3134G>C
  • NM_001407652.1:c.3260G>C
  • NM_001407653.1:c.3182G>C
  • NM_001407654.1:c.3182G>C
  • NM_001407655.1:c.3182G>C
  • NM_001407656.1:c.3182G>C
  • NM_001407657.1:c.3182G>C
  • NM_001407658.1:c.3182G>C
  • NM_001407659.1:c.3179G>C
  • NM_001407660.1:c.3179G>C
  • NM_001407661.1:c.3179G>C
  • NM_001407662.1:c.3179G>C
  • NM_001407663.1:c.3182G>C
  • NM_001407664.1:c.3137G>C
  • NM_001407665.1:c.3137G>C
  • NM_001407666.1:c.3137G>C
  • NM_001407667.1:c.3137G>C
  • NM_001407668.1:c.3137G>C
  • NM_001407669.1:c.3137G>C
  • NM_001407670.1:c.3134G>C
  • NM_001407671.1:c.3134G>C
  • NM_001407672.1:c.3134G>C
  • NM_001407673.1:c.3134G>C
  • NM_001407674.1:c.3137G>C
  • NM_001407675.1:c.3137G>C
  • NM_001407676.1:c.3137G>C
  • NM_001407677.1:c.3137G>C
  • NM_001407678.1:c.3137G>C
  • NM_001407679.1:c.3137G>C
  • NM_001407680.1:c.3137G>C
  • NM_001407681.1:c.3137G>C
  • NM_001407682.1:c.3137G>C
  • NM_001407683.1:c.3137G>C
  • NM_001407684.1:c.3260G>C
  • NM_001407685.1:c.3134G>C
  • NM_001407686.1:c.3134G>C
  • NM_001407687.1:c.3134G>C
  • NM_001407688.1:c.3134G>C
  • NM_001407689.1:c.3134G>C
  • NM_001407690.1:c.3134G>C
  • NM_001407691.1:c.3134G>C
  • NM_001407692.1:c.3119G>C
  • NM_001407694.1:c.3119G>C
  • NM_001407695.1:c.3119G>C
  • NM_001407696.1:c.3119G>C
  • NM_001407697.1:c.3119G>C
  • NM_001407698.1:c.3119G>C
  • NM_001407724.1:c.3119G>C
  • NM_001407725.1:c.3119G>C
  • NM_001407726.1:c.3119G>C
  • NM_001407727.1:c.3119G>C
  • NM_001407728.1:c.3119G>C
  • NM_001407729.1:c.3119G>C
  • NM_001407730.1:c.3119G>C
  • NM_001407731.1:c.3119G>C
  • NM_001407732.1:c.3119G>C
  • NM_001407733.1:c.3119G>C
  • NM_001407734.1:c.3119G>C
  • NM_001407735.1:c.3119G>C
  • NM_001407736.1:c.3119G>C
  • NM_001407737.1:c.3119G>C
  • NM_001407738.1:c.3119G>C
  • NM_001407739.1:c.3119G>C
  • NM_001407740.1:c.3116G>C
  • NM_001407741.1:c.3116G>C
  • NM_001407742.1:c.3116G>C
  • NM_001407743.1:c.3116G>C
  • NM_001407744.1:c.3116G>C
  • NM_001407745.1:c.3116G>C
  • NM_001407746.1:c.3116G>C
  • NM_001407747.1:c.3116G>C
  • NM_001407748.1:c.3116G>C
  • NM_001407749.1:c.3116G>C
  • NM_001407750.1:c.3119G>C
  • NM_001407751.1:c.3119G>C
  • NM_001407752.1:c.3119G>C
  • NM_001407838.1:c.3116G>C
  • NM_001407839.1:c.3116G>C
  • NM_001407841.1:c.3116G>C
  • NM_001407842.1:c.3116G>C
  • NM_001407843.1:c.3116G>C
  • NM_001407844.1:c.3116G>C
  • NM_001407845.1:c.3116G>C
  • NM_001407846.1:c.3116G>C
  • NM_001407847.1:c.3116G>C
  • NM_001407848.1:c.3116G>C
  • NM_001407849.1:c.3116G>C
  • NM_001407850.1:c.3119G>C
  • NM_001407851.1:c.3119G>C
  • NM_001407852.1:c.3119G>C
  • NM_001407853.1:c.3047G>C
  • NM_001407854.1:c.3260G>C
  • NM_001407858.1:c.3260G>C
  • NM_001407859.1:c.3260G>C
  • NM_001407860.1:c.3257G>C
  • NM_001407861.1:c.3257G>C
  • NM_001407862.1:c.3059G>C
  • NM_001407863.1:c.3137G>C
  • NM_001407874.1:c.3056G>C
  • NM_001407875.1:c.3056G>C
  • NM_001407879.1:c.3050G>C
  • NM_001407881.1:c.3050G>C
  • NM_001407882.1:c.3050G>C
  • NM_001407884.1:c.3050G>C
  • NM_001407885.1:c.3050G>C
  • NM_001407886.1:c.3050G>C
  • NM_001407887.1:c.3050G>C
  • NM_001407889.1:c.3050G>C
  • NM_001407894.1:c.3047G>C
  • NM_001407895.1:c.3047G>C
  • NM_001407896.1:c.3047G>C
  • NM_001407897.1:c.3047G>C
  • NM_001407898.1:c.3047G>C
  • NM_001407899.1:c.3047G>C
  • NM_001407900.1:c.3050G>C
  • NM_001407902.1:c.3050G>C
  • NM_001407904.1:c.3050G>C
  • NM_001407906.1:c.3050G>C
  • NM_001407907.1:c.3050G>C
  • NM_001407908.1:c.3050G>C
  • NM_001407909.1:c.3050G>C
  • NM_001407910.1:c.3050G>C
  • NM_001407915.1:c.3047G>C
  • NM_001407916.1:c.3047G>C
  • NM_001407917.1:c.3047G>C
  • NM_001407918.1:c.3047G>C
  • NM_001407919.1:c.3137G>C
  • NM_001407920.1:c.2996G>C
  • NM_001407921.1:c.2996G>C
  • NM_001407922.1:c.2996G>C
  • NM_001407923.1:c.2996G>C
  • NM_001407924.1:c.2996G>C
  • NM_001407925.1:c.2996G>C
  • NM_001407926.1:c.2996G>C
  • NM_001407927.1:c.2996G>C
  • NM_001407928.1:c.2996G>C
  • NM_001407929.1:c.2996G>C
  • NM_001407930.1:c.2993G>C
  • NM_001407931.1:c.2993G>C
  • NM_001407932.1:c.2993G>C
  • NM_001407933.1:c.2996G>C
  • NM_001407934.1:c.2993G>C
  • NM_001407935.1:c.2996G>C
  • NM_001407936.1:c.2993G>C
  • NM_001407937.1:c.3137G>C
  • NM_001407938.1:c.3137G>C
  • NM_001407939.1:c.3137G>C
  • NM_001407940.1:c.3134G>C
  • NM_001407941.1:c.3134G>C
  • NM_001407942.1:c.3119G>C
  • NM_001407943.1:c.3116G>C
  • NM_001407944.1:c.3119G>C
  • NM_001407945.1:c.3119G>C
  • NM_001407946.1:c.2927G>C
  • NM_001407947.1:c.2927G>C
  • NM_001407948.1:c.2927G>C
  • NM_001407949.1:c.2927G>C
  • NM_001407950.1:c.2927G>C
  • NM_001407951.1:c.2927G>C
  • NM_001407952.1:c.2927G>C
  • NM_001407953.1:c.2927G>C
  • NM_001407954.1:c.2924G>C
  • NM_001407955.1:c.2924G>C
  • NM_001407956.1:c.2924G>C
  • NM_001407957.1:c.2927G>C
  • NM_001407958.1:c.2924G>C
  • NM_001407959.1:c.2879G>C
  • NM_001407960.1:c.2879G>C
  • NM_001407962.1:c.2876G>C
  • NM_001407963.1:c.2879G>C
  • NM_001407964.1:c.3116G>C
  • NM_001407965.1:c.2756G>C
  • NM_001407966.1:c.2372G>C
  • NM_001407967.1:c.2372G>C
  • NM_001407968.1:c.788-132G>C
  • NM_001407969.1:c.788-132G>C
  • NM_001407970.1:c.788-1239G>C
  • NM_001407971.1:c.788-1239G>C
  • NM_001407972.1:c.785-1239G>C
  • NM_001407973.1:c.788-1239G>C
  • NM_001407974.1:c.788-1239G>C
  • NM_001407975.1:c.788-1239G>C
  • NM_001407976.1:c.788-1239G>C
  • NM_001407977.1:c.788-1239G>C
  • NM_001407978.1:c.788-1239G>C
  • NM_001407979.1:c.788-1239G>C
  • NM_001407980.1:c.788-1239G>C
  • NM_001407981.1:c.788-1239G>C
  • NM_001407982.1:c.788-1239G>C
  • NM_001407983.1:c.788-1239G>C
  • NM_001407984.1:c.785-1239G>C
  • NM_001407985.1:c.785-1239G>C
  • NM_001407986.1:c.785-1239G>C
  • NM_001407990.1:c.788-1239G>C
  • NM_001407991.1:c.785-1239G>C
  • NM_001407992.1:c.785-1239G>C
  • NM_001407993.1:c.788-1239G>C
  • NM_001408392.1:c.785-1239G>C
  • NM_001408396.1:c.785-1239G>C
  • NM_001408397.1:c.785-1239G>C
  • NM_001408398.1:c.785-1239G>C
  • NM_001408399.1:c.785-1239G>C
  • NM_001408400.1:c.785-1239G>C
  • NM_001408401.1:c.785-1239G>C
  • NM_001408402.1:c.785-1239G>C
  • NM_001408403.1:c.788-1239G>C
  • NM_001408404.1:c.788-1239G>C
  • NM_001408406.1:c.791-1248G>C
  • NM_001408407.1:c.785-1239G>C
  • NM_001408408.1:c.779-1239G>C
  • NM_001408409.1:c.710-1239G>C
  • NM_001408410.1:c.647-1239G>C
  • NM_001408411.1:c.710-1239G>C
  • NM_001408412.1:c.710-1239G>C
  • NM_001408413.1:c.707-1239G>C
  • NM_001408414.1:c.710-1239G>C
  • NM_001408415.1:c.710-1239G>C
  • NM_001408416.1:c.707-1239G>C
  • NM_001408418.1:c.671-1239G>C
  • NM_001408419.1:c.671-1239G>C
  • NM_001408420.1:c.671-1239G>C
  • NM_001408421.1:c.668-1239G>C
  • NM_001408422.1:c.671-1239G>C
  • NM_001408423.1:c.671-1239G>C
  • NM_001408424.1:c.668-1239G>C
  • NM_001408425.1:c.665-1239G>C
  • NM_001408426.1:c.665-1239G>C
  • NM_001408427.1:c.665-1239G>C
  • NM_001408428.1:c.665-1239G>C
  • NM_001408429.1:c.665-1239G>C
  • NM_001408430.1:c.665-1239G>C
  • NM_001408431.1:c.668-1239G>C
  • NM_001408432.1:c.662-1239G>C
  • NM_001408433.1:c.662-1239G>C
  • NM_001408434.1:c.662-1239G>C
  • NM_001408435.1:c.662-1239G>C
  • NM_001408436.1:c.665-1239G>C
  • NM_001408437.1:c.665-1239G>C
  • NM_001408438.1:c.665-1239G>C
  • NM_001408439.1:c.665-1239G>C
  • NM_001408440.1:c.665-1239G>C
  • NM_001408441.1:c.665-1239G>C
  • NM_001408442.1:c.665-1239G>C
  • NM_001408443.1:c.665-1239G>C
  • NM_001408444.1:c.665-1239G>C
  • NM_001408445.1:c.662-1239G>C
  • NM_001408446.1:c.662-1239G>C
  • NM_001408447.1:c.662-1239G>C
  • NM_001408448.1:c.662-1239G>C
  • NM_001408450.1:c.662-1239G>C
  • NM_001408451.1:c.653-1239G>C
  • NM_001408452.1:c.647-1239G>C
  • NM_001408453.1:c.647-1239G>C
  • NM_001408454.1:c.647-1239G>C
  • NM_001408455.1:c.647-1239G>C
  • NM_001408456.1:c.647-1239G>C
  • NM_001408457.1:c.647-1239G>C
  • NM_001408458.1:c.647-1239G>C
  • NM_001408459.1:c.647-1239G>C
  • NM_001408460.1:c.647-1239G>C
  • NM_001408461.1:c.647-1239G>C
  • NM_001408462.1:c.644-1239G>C
  • NM_001408463.1:c.644-1239G>C
  • NM_001408464.1:c.644-1239G>C
  • NM_001408465.1:c.644-1239G>C
  • NM_001408466.1:c.647-1239G>C
  • NM_001408467.1:c.647-1239G>C
  • NM_001408468.1:c.644-1239G>C
  • NM_001408469.1:c.647-1239G>C
  • NM_001408470.1:c.644-1239G>C
  • NM_001408472.1:c.788-1239G>C
  • NM_001408473.1:c.785-1239G>C
  • NM_001408474.1:c.587-1239G>C
  • NM_001408475.1:c.584-1239G>C
  • NM_001408476.1:c.587-1239G>C
  • NM_001408478.1:c.578-1239G>C
  • NM_001408479.1:c.578-1239G>C
  • NM_001408480.1:c.578-1239G>C
  • NM_001408481.1:c.578-1239G>C
  • NM_001408482.1:c.578-1239G>C
  • NM_001408483.1:c.578-1239G>C
  • NM_001408484.1:c.578-1239G>C
  • NM_001408485.1:c.578-1239G>C
  • NM_001408489.1:c.578-1239G>C
  • NM_001408490.1:c.575-1239G>C
  • NM_001408491.1:c.575-1239G>C
  • NM_001408492.1:c.578-1239G>C
  • NM_001408493.1:c.575-1239G>C
  • NM_001408494.1:c.548-1239G>C
  • NM_001408495.1:c.545-1239G>C
  • NM_001408496.1:c.524-1239G>C
  • NM_001408497.1:c.524-1239G>C
  • NM_001408498.1:c.524-1239G>C
  • NM_001408499.1:c.524-1239G>C
  • NM_001408500.1:c.524-1239G>C
  • NM_001408501.1:c.524-1239G>C
  • NM_001408502.1:c.455-1239G>C
  • NM_001408503.1:c.521-1239G>C
  • NM_001408504.1:c.521-1239G>C
  • NM_001408505.1:c.521-1239G>C
  • NM_001408506.1:c.461-1239G>C
  • NM_001408507.1:c.461-1239G>C
  • NM_001408508.1:c.452-1239G>C
  • NM_001408509.1:c.452-1239G>C
  • NM_001408510.1:c.407-1239G>C
  • NM_001408511.1:c.404-1239G>C
  • NM_001408512.1:c.284-1239G>C
  • NM_001408513.1:c.578-1239G>C
  • NM_001408514.1:c.578-1239G>C
  • NM_007294.4:c.3260G>CMANE SELECT
  • NM_007297.4:c.3119G>C
  • NM_007298.4:c.788-1239G>C
  • NM_007299.4:c.788-1239G>C
  • NM_007300.4:c.3260G>C
  • NP_001394500.1:p.Gly1016Ala
  • NP_001394510.1:p.Gly1087Ala
  • NP_001394511.1:p.Gly1087Ala
  • NP_001394512.1:p.Gly1087Ala
  • NP_001394514.1:p.Gly1087Ala
  • NP_001394516.1:p.Gly1086Ala
  • NP_001394519.1:p.Gly1086Ala
  • NP_001394520.1:p.Gly1086Ala
  • NP_001394522.1:p.Gly1087Ala
  • NP_001394523.1:p.Gly1087Ala
  • NP_001394525.1:p.Gly1087Ala
  • NP_001394526.1:p.Gly1087Ala
  • NP_001394527.1:p.Gly1087Ala
  • NP_001394531.1:p.Gly1087Ala
  • NP_001394532.1:p.Gly1087Ala
  • NP_001394534.1:p.Gly1087Ala
  • NP_001394539.1:p.Gly1086Ala
  • NP_001394540.1:p.Gly1086Ala
  • NP_001394541.1:p.Gly1086Ala
  • NP_001394542.1:p.Gly1086Ala
  • NP_001394543.1:p.Gly1086Ala
  • NP_001394544.1:p.Gly1086Ala
  • NP_001394545.1:p.Gly1087Ala
  • NP_001394546.1:p.Gly1087Ala
  • NP_001394547.1:p.Gly1087Ala
  • NP_001394548.1:p.Gly1087Ala
  • NP_001394549.1:p.Gly1087Ala
  • NP_001394550.1:p.Gly1087Ala
  • NP_001394551.1:p.Gly1087Ala
  • NP_001394552.1:p.Gly1087Ala
  • NP_001394553.1:p.Gly1087Ala
  • NP_001394554.1:p.Gly1087Ala
  • NP_001394555.1:p.Gly1087Ala
  • NP_001394556.1:p.Gly1086Ala
  • NP_001394557.1:p.Gly1086Ala
  • NP_001394558.1:p.Gly1086Ala
  • NP_001394559.1:p.Gly1086Ala
  • NP_001394560.1:p.Gly1086Ala
  • NP_001394561.1:p.Gly1086Ala
  • NP_001394562.1:p.Gly1086Ala
  • NP_001394563.1:p.Gly1086Ala
  • NP_001394564.1:p.Gly1086Ala
  • NP_001394565.1:p.Gly1086Ala
  • NP_001394566.1:p.Gly1086Ala
  • NP_001394567.1:p.Gly1086Ala
  • NP_001394568.1:p.Gly1087Ala
  • NP_001394569.1:p.Gly1087Ala
  • NP_001394570.1:p.Gly1087Ala
  • NP_001394571.1:p.Gly1087Ala
  • NP_001394573.1:p.Gly1086Ala
  • NP_001394574.1:p.Gly1086Ala
  • NP_001394575.1:p.Gly1084Ala
  • NP_001394576.1:p.Gly1084Ala
  • NP_001394577.1:p.Gly1046Ala
  • NP_001394578.1:p.Gly1045Ala
  • NP_001394581.1:p.Gly1087Ala
  • NP_001394582.1:p.Gly1061Ala
  • NP_001394583.1:p.Gly1061Ala
  • NP_001394584.1:p.Gly1061Ala
  • NP_001394585.1:p.Gly1061Ala
  • NP_001394586.1:p.Gly1061Ala
  • NP_001394587.1:p.Gly1061Ala
  • NP_001394588.1:p.Gly1060Ala
  • NP_001394589.1:p.Gly1060Ala
  • NP_001394590.1:p.Gly1060Ala
  • NP_001394591.1:p.Gly1060Ala
  • NP_001394592.1:p.Gly1061Ala
  • NP_001394593.1:p.Gly1046Ala
  • NP_001394594.1:p.Gly1046Ala
  • NP_001394595.1:p.Gly1046Ala
  • NP_001394596.1:p.Gly1046Ala
  • NP_001394597.1:p.Gly1046Ala
  • NP_001394598.1:p.Gly1046Ala
  • NP_001394599.1:p.Gly1045Ala
  • NP_001394600.1:p.Gly1045Ala
  • NP_001394601.1:p.Gly1045Ala
  • NP_001394602.1:p.Gly1045Ala
  • NP_001394603.1:p.Gly1046Ala
  • NP_001394604.1:p.Gly1046Ala
  • NP_001394605.1:p.Gly1046Ala
  • NP_001394606.1:p.Gly1046Ala
  • NP_001394607.1:p.Gly1046Ala
  • NP_001394608.1:p.Gly1046Ala
  • NP_001394609.1:p.Gly1046Ala
  • NP_001394610.1:p.Gly1046Ala
  • NP_001394611.1:p.Gly1046Ala
  • NP_001394612.1:p.Gly1046Ala
  • NP_001394613.1:p.Gly1087Ala
  • NP_001394614.1:p.Gly1045Ala
  • NP_001394615.1:p.Gly1045Ala
  • NP_001394616.1:p.Gly1045Ala
  • NP_001394617.1:p.Gly1045Ala
  • NP_001394618.1:p.Gly1045Ala
  • NP_001394619.1:p.Gly1045Ala
  • NP_001394620.1:p.Gly1045Ala
  • NP_001394621.1:p.Gly1040Ala
  • NP_001394623.1:p.Gly1040Ala
  • NP_001394624.1:p.Gly1040Ala
  • NP_001394625.1:p.Gly1040Ala
  • NP_001394626.1:p.Gly1040Ala
  • NP_001394627.1:p.Gly1040Ala
  • NP_001394653.1:p.Gly1040Ala
  • NP_001394654.1:p.Gly1040Ala
  • NP_001394655.1:p.Gly1040Ala
  • NP_001394656.1:p.Gly1040Ala
  • NP_001394657.1:p.Gly1040Ala
  • NP_001394658.1:p.Gly1040Ala
  • NP_001394659.1:p.Gly1040Ala
  • NP_001394660.1:p.Gly1040Ala
  • NP_001394661.1:p.Gly1040Ala
  • NP_001394662.1:p.Gly1040Ala
  • NP_001394663.1:p.Gly1040Ala
  • NP_001394664.1:p.Gly1040Ala
  • NP_001394665.1:p.Gly1040Ala
  • NP_001394666.1:p.Gly1040Ala
  • NP_001394667.1:p.Gly1040Ala
  • NP_001394668.1:p.Gly1040Ala
  • NP_001394669.1:p.Gly1039Ala
  • NP_001394670.1:p.Gly1039Ala
  • NP_001394671.1:p.Gly1039Ala
  • NP_001394672.1:p.Gly1039Ala
  • NP_001394673.1:p.Gly1039Ala
  • NP_001394674.1:p.Gly1039Ala
  • NP_001394675.1:p.Gly1039Ala
  • NP_001394676.1:p.Gly1039Ala
  • NP_001394677.1:p.Gly1039Ala
  • NP_001394678.1:p.Gly1039Ala
  • NP_001394679.1:p.Gly1040Ala
  • NP_001394680.1:p.Gly1040Ala
  • NP_001394681.1:p.Gly1040Ala
  • NP_001394767.1:p.Gly1039Ala
  • NP_001394768.1:p.Gly1039Ala
  • NP_001394770.1:p.Gly1039Ala
  • NP_001394771.1:p.Gly1039Ala
  • NP_001394772.1:p.Gly1039Ala
  • NP_001394773.1:p.Gly1039Ala
  • NP_001394774.1:p.Gly1039Ala
  • NP_001394775.1:p.Gly1039Ala
  • NP_001394776.1:p.Gly1039Ala
  • NP_001394777.1:p.Gly1039Ala
  • NP_001394778.1:p.Gly1039Ala
  • NP_001394779.1:p.Gly1040Ala
  • NP_001394780.1:p.Gly1040Ala
  • NP_001394781.1:p.Gly1040Ala
  • NP_001394782.1:p.Gly1016Ala
  • NP_001394783.1:p.Gly1087Ala
  • NP_001394787.1:p.Gly1087Ala
  • NP_001394788.1:p.Gly1087Ala
  • NP_001394789.1:p.Gly1086Ala
  • NP_001394790.1:p.Gly1086Ala
  • NP_001394791.1:p.Gly1020Ala
  • NP_001394792.1:p.Gly1046Ala
  • NP_001394803.1:p.Gly1019Ala
  • NP_001394804.1:p.Gly1019Ala
  • NP_001394808.1:p.Gly1017Ala
  • NP_001394810.1:p.Gly1017Ala
  • NP_001394811.1:p.Gly1017Ala
  • NP_001394813.1:p.Gly1017Ala
  • NP_001394814.1:p.Gly1017Ala
  • NP_001394815.1:p.Gly1017Ala
  • NP_001394816.1:p.Gly1017Ala
  • NP_001394818.1:p.Gly1017Ala
  • NP_001394823.1:p.Gly1016Ala
  • NP_001394824.1:p.Gly1016Ala
  • NP_001394825.1:p.Gly1016Ala
  • NP_001394826.1:p.Gly1016Ala
  • NP_001394827.1:p.Gly1016Ala
  • NP_001394828.1:p.Gly1016Ala
  • NP_001394829.1:p.Gly1017Ala
  • NP_001394831.1:p.Gly1017Ala
  • NP_001394833.1:p.Gly1017Ala
  • NP_001394835.1:p.Gly1017Ala
  • NP_001394836.1:p.Gly1017Ala
  • NP_001394837.1:p.Gly1017Ala
  • NP_001394838.1:p.Gly1017Ala
  • NP_001394839.1:p.Gly1017Ala
  • NP_001394844.1:p.Gly1016Ala
  • NP_001394845.1:p.Gly1016Ala
  • NP_001394846.1:p.Gly1016Ala
  • NP_001394847.1:p.Gly1016Ala
  • NP_001394848.1:p.Gly1046Ala
  • NP_001394849.1:p.Gly999Ala
  • NP_001394850.1:p.Gly999Ala
  • NP_001394851.1:p.Gly999Ala
  • NP_001394852.1:p.Gly999Ala
  • NP_001394853.1:p.Gly999Ala
  • NP_001394854.1:p.Gly999Ala
  • NP_001394855.1:p.Gly999Ala
  • NP_001394856.1:p.Gly999Ala
  • NP_001394857.1:p.Gly999Ala
  • NP_001394858.1:p.Gly999Ala
  • NP_001394859.1:p.Gly998Ala
  • NP_001394860.1:p.Gly998Ala
  • NP_001394861.1:p.Gly998Ala
  • NP_001394862.1:p.Gly999Ala
  • NP_001394863.1:p.Gly998Ala
  • NP_001394864.1:p.Gly999Ala
  • NP_001394865.1:p.Gly998Ala
  • NP_001394866.1:p.Gly1046Ala
  • NP_001394867.1:p.Gly1046Ala
  • NP_001394868.1:p.Gly1046Ala
  • NP_001394869.1:p.Gly1045Ala
  • NP_001394870.1:p.Gly1045Ala
  • NP_001394871.1:p.Gly1040Ala
  • NP_001394872.1:p.Gly1039Ala
  • NP_001394873.1:p.Gly1040Ala
  • NP_001394874.1:p.Gly1040Ala
  • NP_001394875.1:p.Gly976Ala
  • NP_001394876.1:p.Gly976Ala
  • NP_001394877.1:p.Gly976Ala
  • NP_001394878.1:p.Gly976Ala
  • NP_001394879.1:p.Gly976Ala
  • NP_001394880.1:p.Gly976Ala
  • NP_001394881.1:p.Gly976Ala
  • NP_001394882.1:p.Gly976Ala
  • NP_001394883.1:p.Gly975Ala
  • NP_001394884.1:p.Gly975Ala
  • NP_001394885.1:p.Gly975Ala
  • NP_001394886.1:p.Gly976Ala
  • NP_001394887.1:p.Gly975Ala
  • NP_001394888.1:p.Gly960Ala
  • NP_001394889.1:p.Gly960Ala
  • NP_001394891.1:p.Gly959Ala
  • NP_001394892.1:p.Gly960Ala
  • NP_001394893.1:p.Gly1039Ala
  • NP_001394894.1:p.Gly919Ala
  • NP_001394895.1:p.Gly791Ala
  • NP_001394896.1:p.Gly791Ala
  • NP_009225.1:p.Gly1087Ala
  • NP_009225.1:p.Gly1087Ala
  • NP_009228.2:p.Gly1040Ala
  • NP_009231.2:p.Gly1087Ala
  • LRG_292t1:c.3260G>C
  • LRG_292:g.125713G>C
  • LRG_292p1:p.Gly1087Ala
  • NC_000017.10:g.41244288C>G
  • NM_007294.3:c.3260G>C
  • NR_027676.1:n.3396G>C
  • U14680.1:n.3379G>C
  • p.G1087A
Protein change:
G1016A
Links:
dbSNP: rs80357172
NCBI 1000 Genomes Browser:
rs80357172
Molecular consequence:
  • NM_001407968.1:c.788-132G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.788-132G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.791-1248G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.779-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.710-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.710-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.710-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.707-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.710-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.710-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.707-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.671-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.671-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.671-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.668-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.671-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.671-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.668-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.668-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.662-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.662-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.662-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.662-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.665-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.662-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.662-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.662-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.662-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.662-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.653-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.644-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.644-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.644-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.644-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.644-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.647-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.644-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.785-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.587-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.584-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.587-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.575-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.575-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.575-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.548-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.545-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.524-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.524-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.524-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.524-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.524-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.524-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.455-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.521-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.521-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.521-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.461-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.461-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.452-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.452-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.407-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.404-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.284-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.578-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.788-1239G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.3251G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.3251G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.3182G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.3182G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.3182G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.3182G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.3182G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.3182G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.3179G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.3179G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.3179G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.3179G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.3182G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.3257G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.3059G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.3056G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.3056G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.3050G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.3047G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.2993G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.2993G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.2993G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.2993G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.2996G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.2993G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.3137G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.3134G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.2927G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.2927G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.2927G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.2927G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.2927G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.2927G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.2927G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.2927G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.2924G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.2924G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.2924G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.2927G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.2924G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.2879G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.2879G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.2876G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.2879G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.3116G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.2756G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.2372G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.2372G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.3119G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.3260G>C - missense variant - [Sequence Ontology: SO:0001583]
Observations:
2

Condition(s)

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

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000144693Breast Cancer Information Core (BIC) (BRCA1)
no assertion criteria provided
Uncertain significance
(Dec 23, 2003) 		germlineclinical testing

SCV004815581All of Us Research Program, National Institutes of Health
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain Significance
(Mar 4, 2023) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot provided108544not providedclinical testing
Western Europeangermlineyes1not providednot providednot providednot providedclinical testing

Citations

PubMed

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

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

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

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Breast Cancer Information Core (BIC) (BRCA1), SCV000144693.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1Western European1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

From All of Us Research Program, National Institutes of Health, SCV004815581.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

This missense variant replaces glycine with alanine at codon 1087 of the BRCA1 protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with hereditary cancer in the literature. This variant has been identified in 1/250540 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown108544not providednot provided1not providednot providednot provided

Last Updated: Oct 8, 2024