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NM_007294.4(BRCA1):c.3221G>C (p.Arg1074Thr) AND Hereditary breast ovarian cancer syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 8, 2022
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:
RCV000205205.10

Allele description [Variation Report for NM_007294.4(BRCA1):c.3221G>C (p.Arg1074Thr)]

NM_007294.4(BRCA1):c.3221G>C (p.Arg1074Thr)

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.3221G>C (p.Arg1074Thr)
HGVS:
  • NC_000017.11:g.43092310C>G
  • NG_005905.2:g.125674G>C
  • NG_087068.1:g.1292C>G
  • NM_001407571.1:c.3008G>C
  • NM_001407581.1:c.3221G>C
  • NM_001407582.1:c.3221G>C
  • NM_001407583.1:c.3221G>C
  • NM_001407585.1:c.3221G>C
  • NM_001407587.1:c.3218G>C
  • NM_001407590.1:c.3218G>C
  • NM_001407591.1:c.3218G>C
  • NM_001407593.1:c.3221G>C
  • NM_001407594.1:c.3221G>C
  • NM_001407596.1:c.3221G>C
  • NM_001407597.1:c.3221G>C
  • NM_001407598.1:c.3221G>C
  • NM_001407602.1:c.3221G>C
  • NM_001407603.1:c.3221G>C
  • NM_001407605.1:c.3221G>C
  • NM_001407610.1:c.3218G>C
  • NM_001407611.1:c.3218G>C
  • NM_001407612.1:c.3218G>C
  • NM_001407613.1:c.3218G>C
  • NM_001407614.1:c.3218G>C
  • NM_001407615.1:c.3218G>C
  • NM_001407616.1:c.3221G>C
  • NM_001407617.1:c.3221G>C
  • NM_001407618.1:c.3221G>C
  • NM_001407619.1:c.3221G>C
  • NM_001407620.1:c.3221G>C
  • NM_001407621.1:c.3221G>C
  • NM_001407622.1:c.3221G>C
  • NM_001407623.1:c.3221G>C
  • NM_001407624.1:c.3221G>C
  • NM_001407625.1:c.3221G>C
  • NM_001407626.1:c.3221G>C
  • NM_001407627.1:c.3218G>C
  • NM_001407628.1:c.3218G>C
  • NM_001407629.1:c.3218G>C
  • NM_001407630.1:c.3218G>C
  • NM_001407631.1:c.3218G>C
  • NM_001407632.1:c.3218G>C
  • NM_001407633.1:c.3218G>C
  • NM_001407634.1:c.3218G>C
  • NM_001407635.1:c.3218G>C
  • NM_001407636.1:c.3218G>C
  • NM_001407637.1:c.3218G>C
  • NM_001407638.1:c.3218G>C
  • NM_001407639.1:c.3221G>C
  • NM_001407640.1:c.3221G>C
  • NM_001407641.1:c.3221G>C
  • NM_001407642.1:c.3221G>C
  • NM_001407644.1:c.3218G>C
  • NM_001407645.1:c.3218G>C
  • NM_001407646.1:c.3212G>C
  • NM_001407647.1:c.3212G>C
  • NM_001407648.1:c.3098G>C
  • NM_001407649.1:c.3095G>C
  • NM_001407652.1:c.3221G>C
  • NM_001407653.1:c.3143G>C
  • NM_001407654.1:c.3143G>C
  • NM_001407655.1:c.3143G>C
  • NM_001407656.1:c.3143G>C
  • NM_001407657.1:c.3143G>C
  • NM_001407658.1:c.3143G>C
  • NM_001407659.1:c.3140G>C
  • NM_001407660.1:c.3140G>C
  • NM_001407661.1:c.3140G>C
  • NM_001407662.1:c.3140G>C
  • NM_001407663.1:c.3143G>C
  • NM_001407664.1:c.3098G>C
  • NM_001407665.1:c.3098G>C
  • NM_001407666.1:c.3098G>C
  • NM_001407667.1:c.3098G>C
  • NM_001407668.1:c.3098G>C
  • NM_001407669.1:c.3098G>C
  • NM_001407670.1:c.3095G>C
  • NM_001407671.1:c.3095G>C
  • NM_001407672.1:c.3095G>C
  • NM_001407673.1:c.3095G>C
  • NM_001407674.1:c.3098G>C
  • NM_001407675.1:c.3098G>C
  • NM_001407676.1:c.3098G>C
  • NM_001407677.1:c.3098G>C
  • NM_001407678.1:c.3098G>C
  • NM_001407679.1:c.3098G>C
  • NM_001407680.1:c.3098G>C
  • NM_001407681.1:c.3098G>C
  • NM_001407682.1:c.3098G>C
  • NM_001407683.1:c.3098G>C
  • NM_001407684.1:c.3221G>C
  • NM_001407685.1:c.3095G>C
  • NM_001407686.1:c.3095G>C
  • NM_001407687.1:c.3095G>C
  • NM_001407688.1:c.3095G>C
  • NM_001407689.1:c.3095G>C
  • NM_001407690.1:c.3095G>C
  • NM_001407691.1:c.3095G>C
  • NM_001407692.1:c.3080G>C
  • NM_001407694.1:c.3080G>C
  • NM_001407695.1:c.3080G>C
  • NM_001407696.1:c.3080G>C
  • NM_001407697.1:c.3080G>C
  • NM_001407698.1:c.3080G>C
  • NM_001407724.1:c.3080G>C
  • NM_001407725.1:c.3080G>C
  • NM_001407726.1:c.3080G>C
  • NM_001407727.1:c.3080G>C
  • NM_001407728.1:c.3080G>C
  • NM_001407729.1:c.3080G>C
  • NM_001407730.1:c.3080G>C
  • NM_001407731.1:c.3080G>C
  • NM_001407732.1:c.3080G>C
  • NM_001407733.1:c.3080G>C
  • NM_001407734.1:c.3080G>C
  • NM_001407735.1:c.3080G>C
  • NM_001407736.1:c.3080G>C
  • NM_001407737.1:c.3080G>C
  • NM_001407738.1:c.3080G>C
  • NM_001407739.1:c.3080G>C
  • NM_001407740.1:c.3077G>C
  • NM_001407741.1:c.3077G>C
  • NM_001407742.1:c.3077G>C
  • NM_001407743.1:c.3077G>C
  • NM_001407744.1:c.3077G>C
  • NM_001407745.1:c.3077G>C
  • NM_001407746.1:c.3077G>C
  • NM_001407747.1:c.3077G>C
  • NM_001407748.1:c.3077G>C
  • NM_001407749.1:c.3077G>C
  • NM_001407750.1:c.3080G>C
  • NM_001407751.1:c.3080G>C
  • NM_001407752.1:c.3080G>C
  • NM_001407838.1:c.3077G>C
  • NM_001407839.1:c.3077G>C
  • NM_001407841.1:c.3077G>C
  • NM_001407842.1:c.3077G>C
  • NM_001407843.1:c.3077G>C
  • NM_001407844.1:c.3077G>C
  • NM_001407845.1:c.3077G>C
  • NM_001407846.1:c.3077G>C
  • NM_001407847.1:c.3077G>C
  • NM_001407848.1:c.3077G>C
  • NM_001407849.1:c.3077G>C
  • NM_001407850.1:c.3080G>C
  • NM_001407851.1:c.3080G>C
  • NM_001407852.1:c.3080G>C
  • NM_001407853.1:c.3008G>C
  • NM_001407854.1:c.3221G>C
  • NM_001407858.1:c.3221G>C
  • NM_001407859.1:c.3221G>C
  • NM_001407860.1:c.3218G>C
  • NM_001407861.1:c.3218G>C
  • NM_001407862.1:c.3020G>C
  • NM_001407863.1:c.3098G>C
  • NM_001407874.1:c.3017G>C
  • NM_001407875.1:c.3017G>C
  • NM_001407879.1:c.3011G>C
  • NM_001407881.1:c.3011G>C
  • NM_001407882.1:c.3011G>C
  • NM_001407884.1:c.3011G>C
  • NM_001407885.1:c.3011G>C
  • NM_001407886.1:c.3011G>C
  • NM_001407887.1:c.3011G>C
  • NM_001407889.1:c.3011G>C
  • NM_001407894.1:c.3008G>C
  • NM_001407895.1:c.3008G>C
  • NM_001407896.1:c.3008G>C
  • NM_001407897.1:c.3008G>C
  • NM_001407898.1:c.3008G>C
  • NM_001407899.1:c.3008G>C
  • NM_001407900.1:c.3011G>C
  • NM_001407902.1:c.3011G>C
  • NM_001407904.1:c.3011G>C
  • NM_001407906.1:c.3011G>C
  • NM_001407907.1:c.3011G>C
  • NM_001407908.1:c.3011G>C
  • NM_001407909.1:c.3011G>C
  • NM_001407910.1:c.3011G>C
  • NM_001407915.1:c.3008G>C
  • NM_001407916.1:c.3008G>C
  • NM_001407917.1:c.3008G>C
  • NM_001407918.1:c.3008G>C
  • NM_001407919.1:c.3098G>C
  • NM_001407920.1:c.2957G>C
  • NM_001407921.1:c.2957G>C
  • NM_001407922.1:c.2957G>C
  • NM_001407923.1:c.2957G>C
  • NM_001407924.1:c.2957G>C
  • NM_001407925.1:c.2957G>C
  • NM_001407926.1:c.2957G>C
  • NM_001407927.1:c.2957G>C
  • NM_001407928.1:c.2957G>C
  • NM_001407929.1:c.2957G>C
  • NM_001407930.1:c.2954G>C
  • NM_001407931.1:c.2954G>C
  • NM_001407932.1:c.2954G>C
  • NM_001407933.1:c.2957G>C
  • NM_001407934.1:c.2954G>C
  • NM_001407935.1:c.2957G>C
  • NM_001407936.1:c.2954G>C
  • NM_001407937.1:c.3098G>C
  • NM_001407938.1:c.3098G>C
  • NM_001407939.1:c.3098G>C
  • NM_001407940.1:c.3095G>C
  • NM_001407941.1:c.3095G>C
  • NM_001407942.1:c.3080G>C
  • NM_001407943.1:c.3077G>C
  • NM_001407944.1:c.3080G>C
  • NM_001407945.1:c.3080G>C
  • NM_001407946.1:c.2888G>C
  • NM_001407947.1:c.2888G>C
  • NM_001407948.1:c.2888G>C
  • NM_001407949.1:c.2888G>C
  • NM_001407950.1:c.2888G>C
  • NM_001407951.1:c.2888G>C
  • NM_001407952.1:c.2888G>C
  • NM_001407953.1:c.2888G>C
  • NM_001407954.1:c.2885G>C
  • NM_001407955.1:c.2885G>C
  • NM_001407956.1:c.2885G>C
  • NM_001407957.1:c.2888G>C
  • NM_001407958.1:c.2885G>C
  • NM_001407959.1:c.2840G>C
  • NM_001407960.1:c.2840G>C
  • NM_001407962.1:c.2837G>C
  • NM_001407963.1:c.2840G>C
  • NM_001407964.1:c.3077G>C
  • NM_001407965.1:c.2717G>C
  • NM_001407966.1:c.2333G>C
  • NM_001407967.1:c.2333G>C
  • NM_001407968.1:c.788-171G>C
  • NM_001407969.1:c.788-171G>C
  • NM_001407970.1:c.788-1278G>C
  • NM_001407971.1:c.788-1278G>C
  • NM_001407972.1:c.785-1278G>C
  • NM_001407973.1:c.788-1278G>C
  • NM_001407974.1:c.788-1278G>C
  • NM_001407975.1:c.788-1278G>C
  • NM_001407976.1:c.788-1278G>C
  • NM_001407977.1:c.788-1278G>C
  • NM_001407978.1:c.788-1278G>C
  • NM_001407979.1:c.788-1278G>C
  • NM_001407980.1:c.788-1278G>C
  • NM_001407981.1:c.788-1278G>C
  • NM_001407982.1:c.788-1278G>C
  • NM_001407983.1:c.788-1278G>C
  • NM_001407984.1:c.785-1278G>C
  • NM_001407985.1:c.785-1278G>C
  • NM_001407986.1:c.785-1278G>C
  • NM_001407990.1:c.788-1278G>C
  • NM_001407991.1:c.785-1278G>C
  • NM_001407992.1:c.785-1278G>C
  • NM_001407993.1:c.788-1278G>C
  • NM_001408392.1:c.785-1278G>C
  • NM_001408396.1:c.785-1278G>C
  • NM_001408397.1:c.785-1278G>C
  • NM_001408398.1:c.785-1278G>C
  • NM_001408399.1:c.785-1278G>C
  • NM_001408400.1:c.785-1278G>C
  • NM_001408401.1:c.785-1278G>C
  • NM_001408402.1:c.785-1278G>C
  • NM_001408403.1:c.788-1278G>C
  • NM_001408404.1:c.788-1278G>C
  • NM_001408406.1:c.791-1287G>C
  • NM_001408407.1:c.785-1278G>C
  • NM_001408408.1:c.779-1278G>C
  • NM_001408409.1:c.710-1278G>C
  • NM_001408410.1:c.647-1278G>C
  • NM_001408411.1:c.710-1278G>C
  • NM_001408412.1:c.710-1278G>C
  • NM_001408413.1:c.707-1278G>C
  • NM_001408414.1:c.710-1278G>C
  • NM_001408415.1:c.710-1278G>C
  • NM_001408416.1:c.707-1278G>C
  • NM_001408418.1:c.671-1278G>C
  • NM_001408419.1:c.671-1278G>C
  • NM_001408420.1:c.671-1278G>C
  • NM_001408421.1:c.668-1278G>C
  • NM_001408422.1:c.671-1278G>C
  • NM_001408423.1:c.671-1278G>C
  • NM_001408424.1:c.668-1278G>C
  • NM_001408425.1:c.665-1278G>C
  • NM_001408426.1:c.665-1278G>C
  • NM_001408427.1:c.665-1278G>C
  • NM_001408428.1:c.665-1278G>C
  • NM_001408429.1:c.665-1278G>C
  • NM_001408430.1:c.665-1278G>C
  • NM_001408431.1:c.668-1278G>C
  • NM_001408432.1:c.662-1278G>C
  • NM_001408433.1:c.662-1278G>C
  • NM_001408434.1:c.662-1278G>C
  • NM_001408435.1:c.662-1278G>C
  • NM_001408436.1:c.665-1278G>C
  • NM_001408437.1:c.665-1278G>C
  • NM_001408438.1:c.665-1278G>C
  • NM_001408439.1:c.665-1278G>C
  • NM_001408440.1:c.665-1278G>C
  • NM_001408441.1:c.665-1278G>C
  • NM_001408442.1:c.665-1278G>C
  • NM_001408443.1:c.665-1278G>C
  • NM_001408444.1:c.665-1278G>C
  • NM_001408445.1:c.662-1278G>C
  • NM_001408446.1:c.662-1278G>C
  • NM_001408447.1:c.662-1278G>C
  • NM_001408448.1:c.662-1278G>C
  • NM_001408450.1:c.662-1278G>C
  • NM_001408451.1:c.653-1278G>C
  • NM_001408452.1:c.647-1278G>C
  • NM_001408453.1:c.647-1278G>C
  • NM_001408454.1:c.647-1278G>C
  • NM_001408455.1:c.647-1278G>C
  • NM_001408456.1:c.647-1278G>C
  • NM_001408457.1:c.647-1278G>C
  • NM_001408458.1:c.647-1278G>C
  • NM_001408459.1:c.647-1278G>C
  • NM_001408460.1:c.647-1278G>C
  • NM_001408461.1:c.647-1278G>C
  • NM_001408462.1:c.644-1278G>C
  • NM_001408463.1:c.644-1278G>C
  • NM_001408464.1:c.644-1278G>C
  • NM_001408465.1:c.644-1278G>C
  • NM_001408466.1:c.647-1278G>C
  • NM_001408467.1:c.647-1278G>C
  • NM_001408468.1:c.644-1278G>C
  • NM_001408469.1:c.647-1278G>C
  • NM_001408470.1:c.644-1278G>C
  • NM_001408472.1:c.788-1278G>C
  • NM_001408473.1:c.785-1278G>C
  • NM_001408474.1:c.587-1278G>C
  • NM_001408475.1:c.584-1278G>C
  • NM_001408476.1:c.587-1278G>C
  • NM_001408478.1:c.578-1278G>C
  • NM_001408479.1:c.578-1278G>C
  • NM_001408480.1:c.578-1278G>C
  • NM_001408481.1:c.578-1278G>C
  • NM_001408482.1:c.578-1278G>C
  • NM_001408483.1:c.578-1278G>C
  • NM_001408484.1:c.578-1278G>C
  • NM_001408485.1:c.578-1278G>C
  • NM_001408489.1:c.578-1278G>C
  • NM_001408490.1:c.575-1278G>C
  • NM_001408491.1:c.575-1278G>C
  • NM_001408492.1:c.578-1278G>C
  • NM_001408493.1:c.575-1278G>C
  • NM_001408494.1:c.548-1278G>C
  • NM_001408495.1:c.545-1278G>C
  • NM_001408496.1:c.524-1278G>C
  • NM_001408497.1:c.524-1278G>C
  • NM_001408498.1:c.524-1278G>C
  • NM_001408499.1:c.524-1278G>C
  • NM_001408500.1:c.524-1278G>C
  • NM_001408501.1:c.524-1278G>C
  • NM_001408502.1:c.455-1278G>C
  • NM_001408503.1:c.521-1278G>C
  • NM_001408504.1:c.521-1278G>C
  • NM_001408505.1:c.521-1278G>C
  • NM_001408506.1:c.461-1278G>C
  • NM_001408507.1:c.461-1278G>C
  • NM_001408508.1:c.452-1278G>C
  • NM_001408509.1:c.452-1278G>C
  • NM_001408510.1:c.407-1278G>C
  • NM_001408511.1:c.404-1278G>C
  • NM_001408512.1:c.284-1278G>C
  • NM_001408513.1:c.578-1278G>C
  • NM_001408514.1:c.578-1278G>C
  • NM_007294.4:c.3221G>CMANE SELECT
  • NM_007297.4:c.3080G>C
  • NM_007298.4:c.788-1278G>C
  • NM_007299.4:c.788-1278G>C
  • NM_007300.4:c.3221G>C
  • NP_001394500.1:p.Arg1003Thr
  • NP_001394510.1:p.Arg1074Thr
  • NP_001394511.1:p.Arg1074Thr
  • NP_001394512.1:p.Arg1074Thr
  • NP_001394514.1:p.Arg1074Thr
  • NP_001394516.1:p.Arg1073Thr
  • NP_001394519.1:p.Arg1073Thr
  • NP_001394520.1:p.Arg1073Thr
  • NP_001394522.1:p.Arg1074Thr
  • NP_001394523.1:p.Arg1074Thr
  • NP_001394525.1:p.Arg1074Thr
  • NP_001394526.1:p.Arg1074Thr
  • NP_001394527.1:p.Arg1074Thr
  • NP_001394531.1:p.Arg1074Thr
  • NP_001394532.1:p.Arg1074Thr
  • NP_001394534.1:p.Arg1074Thr
  • NP_001394539.1:p.Arg1073Thr
  • NP_001394540.1:p.Arg1073Thr
  • NP_001394541.1:p.Arg1073Thr
  • NP_001394542.1:p.Arg1073Thr
  • NP_001394543.1:p.Arg1073Thr
  • NP_001394544.1:p.Arg1073Thr
  • NP_001394545.1:p.Arg1074Thr
  • NP_001394546.1:p.Arg1074Thr
  • NP_001394547.1:p.Arg1074Thr
  • NP_001394548.1:p.Arg1074Thr
  • NP_001394549.1:p.Arg1074Thr
  • NP_001394550.1:p.Arg1074Thr
  • NP_001394551.1:p.Arg1074Thr
  • NP_001394552.1:p.Arg1074Thr
  • NP_001394553.1:p.Arg1074Thr
  • NP_001394554.1:p.Arg1074Thr
  • NP_001394555.1:p.Arg1074Thr
  • NP_001394556.1:p.Arg1073Thr
  • NP_001394557.1:p.Arg1073Thr
  • NP_001394558.1:p.Arg1073Thr
  • NP_001394559.1:p.Arg1073Thr
  • NP_001394560.1:p.Arg1073Thr
  • NP_001394561.1:p.Arg1073Thr
  • NP_001394562.1:p.Arg1073Thr
  • NP_001394563.1:p.Arg1073Thr
  • NP_001394564.1:p.Arg1073Thr
  • NP_001394565.1:p.Arg1073Thr
  • NP_001394566.1:p.Arg1073Thr
  • NP_001394567.1:p.Arg1073Thr
  • NP_001394568.1:p.Arg1074Thr
  • NP_001394569.1:p.Arg1074Thr
  • NP_001394570.1:p.Arg1074Thr
  • NP_001394571.1:p.Arg1074Thr
  • NP_001394573.1:p.Arg1073Thr
  • NP_001394574.1:p.Arg1073Thr
  • NP_001394575.1:p.Arg1071Thr
  • NP_001394576.1:p.Arg1071Thr
  • NP_001394577.1:p.Arg1033Thr
  • NP_001394578.1:p.Arg1032Thr
  • NP_001394581.1:p.Arg1074Thr
  • NP_001394582.1:p.Arg1048Thr
  • NP_001394583.1:p.Arg1048Thr
  • NP_001394584.1:p.Arg1048Thr
  • NP_001394585.1:p.Arg1048Thr
  • NP_001394586.1:p.Arg1048Thr
  • NP_001394587.1:p.Arg1048Thr
  • NP_001394588.1:p.Arg1047Thr
  • NP_001394589.1:p.Arg1047Thr
  • NP_001394590.1:p.Arg1047Thr
  • NP_001394591.1:p.Arg1047Thr
  • NP_001394592.1:p.Arg1048Thr
  • NP_001394593.1:p.Arg1033Thr
  • NP_001394594.1:p.Arg1033Thr
  • NP_001394595.1:p.Arg1033Thr
  • NP_001394596.1:p.Arg1033Thr
  • NP_001394597.1:p.Arg1033Thr
  • NP_001394598.1:p.Arg1033Thr
  • NP_001394599.1:p.Arg1032Thr
  • NP_001394600.1:p.Arg1032Thr
  • NP_001394601.1:p.Arg1032Thr
  • NP_001394602.1:p.Arg1032Thr
  • NP_001394603.1:p.Arg1033Thr
  • NP_001394604.1:p.Arg1033Thr
  • NP_001394605.1:p.Arg1033Thr
  • NP_001394606.1:p.Arg1033Thr
  • NP_001394607.1:p.Arg1033Thr
  • NP_001394608.1:p.Arg1033Thr
  • NP_001394609.1:p.Arg1033Thr
  • NP_001394610.1:p.Arg1033Thr
  • NP_001394611.1:p.Arg1033Thr
  • NP_001394612.1:p.Arg1033Thr
  • NP_001394613.1:p.Arg1074Thr
  • NP_001394614.1:p.Arg1032Thr
  • NP_001394615.1:p.Arg1032Thr
  • NP_001394616.1:p.Arg1032Thr
  • NP_001394617.1:p.Arg1032Thr
  • NP_001394618.1:p.Arg1032Thr
  • NP_001394619.1:p.Arg1032Thr
  • NP_001394620.1:p.Arg1032Thr
  • NP_001394621.1:p.Arg1027Thr
  • NP_001394623.1:p.Arg1027Thr
  • NP_001394624.1:p.Arg1027Thr
  • NP_001394625.1:p.Arg1027Thr
  • NP_001394626.1:p.Arg1027Thr
  • NP_001394627.1:p.Arg1027Thr
  • NP_001394653.1:p.Arg1027Thr
  • NP_001394654.1:p.Arg1027Thr
  • NP_001394655.1:p.Arg1027Thr
  • NP_001394656.1:p.Arg1027Thr
  • NP_001394657.1:p.Arg1027Thr
  • NP_001394658.1:p.Arg1027Thr
  • NP_001394659.1:p.Arg1027Thr
  • NP_001394660.1:p.Arg1027Thr
  • NP_001394661.1:p.Arg1027Thr
  • NP_001394662.1:p.Arg1027Thr
  • NP_001394663.1:p.Arg1027Thr
  • NP_001394664.1:p.Arg1027Thr
  • NP_001394665.1:p.Arg1027Thr
  • NP_001394666.1:p.Arg1027Thr
  • NP_001394667.1:p.Arg1027Thr
  • NP_001394668.1:p.Arg1027Thr
  • NP_001394669.1:p.Arg1026Thr
  • NP_001394670.1:p.Arg1026Thr
  • NP_001394671.1:p.Arg1026Thr
  • NP_001394672.1:p.Arg1026Thr
  • NP_001394673.1:p.Arg1026Thr
  • NP_001394674.1:p.Arg1026Thr
  • NP_001394675.1:p.Arg1026Thr
  • NP_001394676.1:p.Arg1026Thr
  • NP_001394677.1:p.Arg1026Thr
  • NP_001394678.1:p.Arg1026Thr
  • NP_001394679.1:p.Arg1027Thr
  • NP_001394680.1:p.Arg1027Thr
  • NP_001394681.1:p.Arg1027Thr
  • NP_001394767.1:p.Arg1026Thr
  • NP_001394768.1:p.Arg1026Thr
  • NP_001394770.1:p.Arg1026Thr
  • NP_001394771.1:p.Arg1026Thr
  • NP_001394772.1:p.Arg1026Thr
  • NP_001394773.1:p.Arg1026Thr
  • NP_001394774.1:p.Arg1026Thr
  • NP_001394775.1:p.Arg1026Thr
  • NP_001394776.1:p.Arg1026Thr
  • NP_001394777.1:p.Arg1026Thr
  • NP_001394778.1:p.Arg1026Thr
  • NP_001394779.1:p.Arg1027Thr
  • NP_001394780.1:p.Arg1027Thr
  • NP_001394781.1:p.Arg1027Thr
  • NP_001394782.1:p.Arg1003Thr
  • NP_001394783.1:p.Arg1074Thr
  • NP_001394787.1:p.Arg1074Thr
  • NP_001394788.1:p.Arg1074Thr
  • NP_001394789.1:p.Arg1073Thr
  • NP_001394790.1:p.Arg1073Thr
  • NP_001394791.1:p.Arg1007Thr
  • NP_001394792.1:p.Arg1033Thr
  • NP_001394803.1:p.Arg1006Thr
  • NP_001394804.1:p.Arg1006Thr
  • NP_001394808.1:p.Arg1004Thr
  • NP_001394810.1:p.Arg1004Thr
  • NP_001394811.1:p.Arg1004Thr
  • NP_001394813.1:p.Arg1004Thr
  • NP_001394814.1:p.Arg1004Thr
  • NP_001394815.1:p.Arg1004Thr
  • NP_001394816.1:p.Arg1004Thr
  • NP_001394818.1:p.Arg1004Thr
  • NP_001394823.1:p.Arg1003Thr
  • NP_001394824.1:p.Arg1003Thr
  • NP_001394825.1:p.Arg1003Thr
  • NP_001394826.1:p.Arg1003Thr
  • NP_001394827.1:p.Arg1003Thr
  • NP_001394828.1:p.Arg1003Thr
  • NP_001394829.1:p.Arg1004Thr
  • NP_001394831.1:p.Arg1004Thr
  • NP_001394833.1:p.Arg1004Thr
  • NP_001394835.1:p.Arg1004Thr
  • NP_001394836.1:p.Arg1004Thr
  • NP_001394837.1:p.Arg1004Thr
  • NP_001394838.1:p.Arg1004Thr
  • NP_001394839.1:p.Arg1004Thr
  • NP_001394844.1:p.Arg1003Thr
  • NP_001394845.1:p.Arg1003Thr
  • NP_001394846.1:p.Arg1003Thr
  • NP_001394847.1:p.Arg1003Thr
  • NP_001394848.1:p.Arg1033Thr
  • NP_001394849.1:p.Arg986Thr
  • NP_001394850.1:p.Arg986Thr
  • NP_001394851.1:p.Arg986Thr
  • NP_001394852.1:p.Arg986Thr
  • NP_001394853.1:p.Arg986Thr
  • NP_001394854.1:p.Arg986Thr
  • NP_001394855.1:p.Arg986Thr
  • NP_001394856.1:p.Arg986Thr
  • NP_001394857.1:p.Arg986Thr
  • NP_001394858.1:p.Arg986Thr
  • NP_001394859.1:p.Arg985Thr
  • NP_001394860.1:p.Arg985Thr
  • NP_001394861.1:p.Arg985Thr
  • NP_001394862.1:p.Arg986Thr
  • NP_001394863.1:p.Arg985Thr
  • NP_001394864.1:p.Arg986Thr
  • NP_001394865.1:p.Arg985Thr
  • NP_001394866.1:p.Arg1033Thr
  • NP_001394867.1:p.Arg1033Thr
  • NP_001394868.1:p.Arg1033Thr
  • NP_001394869.1:p.Arg1032Thr
  • NP_001394870.1:p.Arg1032Thr
  • NP_001394871.1:p.Arg1027Thr
  • NP_001394872.1:p.Arg1026Thr
  • NP_001394873.1:p.Arg1027Thr
  • NP_001394874.1:p.Arg1027Thr
  • NP_001394875.1:p.Arg963Thr
  • NP_001394876.1:p.Arg963Thr
  • NP_001394877.1:p.Arg963Thr
  • NP_001394878.1:p.Arg963Thr
  • NP_001394879.1:p.Arg963Thr
  • NP_001394880.1:p.Arg963Thr
  • NP_001394881.1:p.Arg963Thr
  • NP_001394882.1:p.Arg963Thr
  • NP_001394883.1:p.Arg962Thr
  • NP_001394884.1:p.Arg962Thr
  • NP_001394885.1:p.Arg962Thr
  • NP_001394886.1:p.Arg963Thr
  • NP_001394887.1:p.Arg962Thr
  • NP_001394888.1:p.Arg947Thr
  • NP_001394889.1:p.Arg947Thr
  • NP_001394891.1:p.Arg946Thr
  • NP_001394892.1:p.Arg947Thr
  • NP_001394893.1:p.Arg1026Thr
  • NP_001394894.1:p.Arg906Thr
  • NP_001394895.1:p.Arg778Thr
  • NP_001394896.1:p.Arg778Thr
  • NP_009225.1:p.Arg1074Thr
  • NP_009225.1:p.Arg1074Thr
  • NP_009228.2:p.Arg1027Thr
  • NP_009231.2:p.Arg1074Thr
  • LRG_292t1:c.3221G>C
  • LRG_292:g.125674G>C
  • LRG_292p1:p.Arg1074Thr
  • NC_000017.10:g.41244327C>G
  • NM_007294.3:c.3221G>C
  • NR_027676.1:n.3357G>C
  • p.R1074T
Protein change:
R1003T
Links:
dbSNP: rs786202155
NCBI 1000 Genomes Browser:
rs786202155
Molecular consequence:
  • NM_001407968.1:c.788-171G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407969.1:c.788-171G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407970.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.791-1287G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.779-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.710-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.710-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.710-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.707-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.710-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.710-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.707-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.671-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.671-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.671-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.668-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.671-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.671-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.668-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.668-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.662-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.662-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.662-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.662-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.665-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.662-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.662-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.662-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.662-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.662-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.653-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.644-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.644-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.644-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.644-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.644-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.647-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.644-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.785-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.587-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.584-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.587-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.575-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.575-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.575-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.548-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.545-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.524-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.524-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.524-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.524-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.524-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.524-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.455-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.521-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.521-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.521-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.461-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.461-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.452-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.452-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.407-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.404-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.284-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.578-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.788-1278G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.3212G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.3212G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.3143G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.3143G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.3143G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.3143G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.3143G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.3143G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.3140G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.3140G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.3140G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.3140G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.3143G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.3218G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.3020G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.3017G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.3017G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.3011G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.3008G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.2954G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.2954G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.2954G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.2954G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.2957G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.2954G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.3098G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.3095G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.2888G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.2888G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.2888G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.2888G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.2888G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.2888G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.2888G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.2888G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.2885G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.2885G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.2885G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.2888G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.2885G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.2840G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.2840G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.2837G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.2840G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.3077G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.2717G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.2333G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.2333G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.3080G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.3221G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hereditary breast ovarian cancer syndrome
Synonyms:
Hereditary breast and ovarian cancer syndrome; Hereditary breast and ovarian cancer; Hereditary breast and ovarian cancer syndrome (HBOC); See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0003582; MeSH: D061325; MedGen: C0677776; Orphanet: 145

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000260402Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Oct 8, 2022) 		germlineclinical testing

PubMed (2)
[See all records that cite these PMIDs]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.

Borg A, Haile RW, Malone KE, Capanu M, Diep A, Törngren T, Teraoka S, Begg CB, Thomas DC, Concannon P, Mellemkjaer L, Bernstein L, Tellhed L, Xue S, Olson ER, Liang X, Dolle J, Børresen-Dale AL, Bernstein JL.

Hum Mutat. 2010 Mar;31(3):E1200-40. doi: 10.1002/humu.21202.

PubMed [citation]
PMID:
20104584
PMCID:
PMC2928257

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000260402.7

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (2)

Description

This sequence change replaces arginine, which is basic and polar, with threonine, which is neutral and polar, at codon 1074 of the BRCA1 protein (p.Arg1074Thr). This variant is present in population databases (rs786202155, gnomAD 0.007%). This missense change has been observed in individual(s) with breast cancer (PMID: 20104584). ClinVar contains an entry for this variant (Variation ID: 185414). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt BRCA1 protein function. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 8, 2024