ClinVar Genomic variation as it relates to human health
NM_007294.4(BRCA1):c.3406C>T (p.Pro1136Ser)
The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.
Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.
Uncertain significance(4); Likely benign(1)
No data submitted for somatic clinical impact
No data submitted for oncogenicity
Variant Details
- Identifiers
-
NM_007294.4(BRCA1):c.3406C>T (p.Pro1136Ser)
Variation ID: 823737 Accession: VCV000823737.15
- Type and length
-
single nucleotide variant, 1 bp
- Location
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Cytogenetic: 17q21.31 17: 43092125 (GRCh38) [ NCBI UCSC ] 17: 41244142 (GRCh37) [ NCBI UCSC ]
- Timeline in ClinVar
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First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.
Last submission Help The date of the most recent submission for each type of classification for this variant.
Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline Mar 16, 2020 May 1, 2024 Mar 23, 2023 - HGVS
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Nucleotide Protein Molecular
consequenceNM_007294.4:c.3406C>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_009225.1:p.Pro1136Ser missense NM_001407571.1:c.3193C>T NP_001394500.1:p.Pro1065Ser missense NM_001407581.1:c.3406C>T NP_001394510.1:p.Pro1136Ser missense NM_001407582.1:c.3406C>T NP_001394511.1:p.Pro1136Ser missense NM_001407583.1:c.3406C>T NP_001394512.1:p.Pro1136Ser missense NM_001407585.1:c.3406C>T NP_001394514.1:p.Pro1136Ser missense NM_001407587.1:c.3403C>T NP_001394516.1:p.Pro1135Ser missense NM_001407590.1:c.3403C>T NP_001394519.1:p.Pro1135Ser missense NM_001407591.1:c.3403C>T NP_001394520.1:p.Pro1135Ser missense NM_001407593.1:c.3406C>T NP_001394522.1:p.Pro1136Ser missense NM_001407594.1:c.3406C>T NP_001394523.1:p.Pro1136Ser missense NM_001407596.1:c.3406C>T NP_001394525.1:p.Pro1136Ser missense NM_001407597.1:c.3406C>T NP_001394526.1:p.Pro1136Ser missense NM_001407598.1:c.3406C>T NP_001394527.1:p.Pro1136Ser missense NM_001407602.1:c.3406C>T NP_001394531.1:p.Pro1136Ser missense NM_001407603.1:c.3406C>T NP_001394532.1:p.Pro1136Ser missense NM_001407605.1:c.3406C>T NP_001394534.1:p.Pro1136Ser missense NM_001407610.1:c.3403C>T NP_001394539.1:p.Pro1135Ser missense NM_001407611.1:c.3403C>T NP_001394540.1:p.Pro1135Ser missense NM_001407612.1:c.3403C>T NP_001394541.1:p.Pro1135Ser missense NM_001407613.1:c.3403C>T NP_001394542.1:p.Pro1135Ser missense NM_001407614.1:c.3403C>T NP_001394543.1:p.Pro1135Ser missense NM_001407615.1:c.3403C>T NP_001394544.1:p.Pro1135Ser missense NM_001407616.1:c.3406C>T NP_001394545.1:p.Pro1136Ser missense NM_001407617.1:c.3406C>T NP_001394546.1:p.Pro1136Ser missense NM_001407618.1:c.3406C>T NP_001394547.1:p.Pro1136Ser missense NM_001407619.1:c.3406C>T NP_001394548.1:p.Pro1136Ser missense NM_001407620.1:c.3406C>T NP_001394549.1:p.Pro1136Ser missense NM_001407621.1:c.3406C>T NP_001394550.1:p.Pro1136Ser missense NM_001407622.1:c.3406C>T NP_001394551.1:p.Pro1136Ser missense NM_001407623.1:c.3406C>T NP_001394552.1:p.Pro1136Ser missense NM_001407624.1:c.3406C>T NP_001394553.1:p.Pro1136Ser missense NM_001407625.1:c.3406C>T NP_001394554.1:p.Pro1136Ser missense NM_001407626.1:c.3406C>T NP_001394555.1:p.Pro1136Ser missense NM_001407627.1:c.3403C>T NP_001394556.1:p.Pro1135Ser missense NM_001407628.1:c.3403C>T NP_001394557.1:p.Pro1135Ser missense NM_001407629.1:c.3403C>T NP_001394558.1:p.Pro1135Ser missense NM_001407630.1:c.3403C>T NP_001394559.1:p.Pro1135Ser missense NM_001407631.1:c.3403C>T NP_001394560.1:p.Pro1135Ser missense NM_001407632.1:c.3403C>T NP_001394561.1:p.Pro1135Ser missense NM_001407633.1:c.3403C>T NP_001394562.1:p.Pro1135Ser missense NM_001407634.1:c.3403C>T NP_001394563.1:p.Pro1135Ser missense NM_001407635.1:c.3403C>T NP_001394564.1:p.Pro1135Ser missense NM_001407636.1:c.3403C>T NP_001394565.1:p.Pro1135Ser missense NM_001407637.1:c.3403C>T NP_001394566.1:p.Pro1135Ser missense NM_001407638.1:c.3403C>T NP_001394567.1:p.Pro1135Ser missense NM_001407639.1:c.3406C>T NP_001394568.1:p.Pro1136Ser missense NM_001407640.1:c.3406C>T NP_001394569.1:p.Pro1136Ser missense NM_001407641.1:c.3406C>T NP_001394570.1:p.Pro1136Ser missense NM_001407642.1:c.3406C>T NP_001394571.1:p.Pro1136Ser missense NM_001407644.1:c.3403C>T NP_001394573.1:p.Pro1135Ser missense NM_001407645.1:c.3403C>T NP_001394574.1:p.Pro1135Ser missense NM_001407646.1:c.3397C>T NP_001394575.1:p.Pro1133Ser missense NM_001407647.1:c.3397C>T NP_001394576.1:p.Pro1133Ser missense NM_001407648.1:c.3283C>T NP_001394577.1:p.Pro1095Ser missense NM_001407649.1:c.3280C>T NP_001394578.1:p.Pro1094Ser missense NM_001407652.1:c.3406C>T NP_001394581.1:p.Pro1136Ser missense NM_001407653.1:c.3328C>T NP_001394582.1:p.Pro1110Ser missense NM_001407654.1:c.3328C>T NP_001394583.1:p.Pro1110Ser missense NM_001407655.1:c.3328C>T NP_001394584.1:p.Pro1110Ser missense NM_001407656.1:c.3328C>T NP_001394585.1:p.Pro1110Ser missense NM_001407657.1:c.3328C>T NP_001394586.1:p.Pro1110Ser missense NM_001407658.1:c.3328C>T NP_001394587.1:p.Pro1110Ser missense NM_001407659.1:c.3325C>T NP_001394588.1:p.Pro1109Ser missense NM_001407660.1:c.3325C>T NP_001394589.1:p.Pro1109Ser missense NM_001407661.1:c.3325C>T NP_001394590.1:p.Pro1109Ser missense NM_001407662.1:c.3325C>T NP_001394591.1:p.Pro1109Ser missense NM_001407663.1:c.3328C>T NP_001394592.1:p.Pro1110Ser missense NM_001407664.1:c.3283C>T NP_001394593.1:p.Pro1095Ser missense NM_001407665.1:c.3283C>T NP_001394594.1:p.Pro1095Ser missense NM_001407666.1:c.3283C>T NP_001394595.1:p.Pro1095Ser missense NM_001407667.1:c.3283C>T NP_001394596.1:p.Pro1095Ser missense NM_001407668.1:c.3283C>T NP_001394597.1:p.Pro1095Ser missense NM_001407669.1:c.3283C>T NP_001394598.1:p.Pro1095Ser missense NM_001407670.1:c.3280C>T NP_001394599.1:p.Pro1094Ser missense NM_001407671.1:c.3280C>T NP_001394600.1:p.Pro1094Ser missense NM_001407672.1:c.3280C>T NP_001394601.1:p.Pro1094Ser missense NM_001407673.1:c.3280C>T NP_001394602.1:p.Pro1094Ser missense NM_001407674.1:c.3283C>T NP_001394603.1:p.Pro1095Ser missense NM_001407675.1:c.3283C>T NP_001394604.1:p.Pro1095Ser missense NM_001407676.1:c.3283C>T NP_001394605.1:p.Pro1095Ser missense NM_001407677.1:c.3283C>T NP_001394606.1:p.Pro1095Ser missense NM_001407678.1:c.3283C>T NP_001394607.1:p.Pro1095Ser missense NM_001407679.1:c.3283C>T NP_001394608.1:p.Pro1095Ser missense NM_001407680.1:c.3283C>T NP_001394609.1:p.Pro1095Ser missense NM_001407681.1:c.3283C>T NP_001394610.1:p.Pro1095Ser missense NM_001407682.1:c.3283C>T NP_001394611.1:p.Pro1095Ser missense NM_001407683.1:c.3283C>T NP_001394612.1:p.Pro1095Ser missense NM_001407684.1:c.3406C>T NP_001394613.1:p.Pro1136Ser missense NM_001407685.1:c.3280C>T NP_001394614.1:p.Pro1094Ser missense NM_001407686.1:c.3280C>T NP_001394615.1:p.Pro1094Ser missense NM_001407687.1:c.3280C>T NP_001394616.1:p.Pro1094Ser missense NM_001407688.1:c.3280C>T NP_001394617.1:p.Pro1094Ser missense NM_001407689.1:c.3280C>T NP_001394618.1:p.Pro1094Ser missense NM_001407690.1:c.3280C>T NP_001394619.1:p.Pro1094Ser missense NM_001407691.1:c.3280C>T NP_001394620.1:p.Pro1094Ser missense NM_001407692.1:c.3265C>T NP_001394621.1:p.Pro1089Ser missense NM_001407694.1:c.3265C>T NP_001394623.1:p.Pro1089Ser missense NM_001407695.1:c.3265C>T NP_001394624.1:p.Pro1089Ser missense NM_001407696.1:c.3265C>T NP_001394625.1:p.Pro1089Ser missense NM_001407697.1:c.3265C>T NP_001394626.1:p.Pro1089Ser missense NM_001407698.1:c.3265C>T NP_001394627.1:p.Pro1089Ser missense NM_001407724.1:c.3265C>T NP_001394653.1:p.Pro1089Ser missense NM_001407725.1:c.3265C>T NP_001394654.1:p.Pro1089Ser missense NM_001407726.1:c.3265C>T NP_001394655.1:p.Pro1089Ser missense NM_001407727.1:c.3265C>T NP_001394656.1:p.Pro1089Ser missense NM_001407728.1:c.3265C>T NP_001394657.1:p.Pro1089Ser missense NM_001407729.1:c.3265C>T NP_001394658.1:p.Pro1089Ser missense NM_001407730.1:c.3265C>T NP_001394659.1:p.Pro1089Ser missense NM_001407731.1:c.3265C>T NP_001394660.1:p.Pro1089Ser missense NM_001407732.1:c.3265C>T NP_001394661.1:p.Pro1089Ser missense NM_001407733.1:c.3265C>T NP_001394662.1:p.Pro1089Ser missense NM_001407734.1:c.3265C>T NP_001394663.1:p.Pro1089Ser missense NM_001407735.1:c.3265C>T NP_001394664.1:p.Pro1089Ser missense NM_001407736.1:c.3265C>T NP_001394665.1:p.Pro1089Ser missense NM_001407737.1:c.3265C>T NP_001394666.1:p.Pro1089Ser missense NM_001407738.1:c.3265C>T NP_001394667.1:p.Pro1089Ser missense NM_001407739.1:c.3265C>T NP_001394668.1:p.Pro1089Ser missense NM_001407740.1:c.3262C>T NP_001394669.1:p.Pro1088Ser missense NM_001407741.1:c.3262C>T NP_001394670.1:p.Pro1088Ser missense NM_001407742.1:c.3262C>T NP_001394671.1:p.Pro1088Ser missense NM_001407743.1:c.3262C>T NP_001394672.1:p.Pro1088Ser missense NM_001407744.1:c.3262C>T NP_001394673.1:p.Pro1088Ser missense NM_001407745.1:c.3262C>T NP_001394674.1:p.Pro1088Ser missense NM_001407746.1:c.3262C>T NP_001394675.1:p.Pro1088Ser missense NM_001407747.1:c.3262C>T NP_001394676.1:p.Pro1088Ser missense NM_001407748.1:c.3262C>T NP_001394677.1:p.Pro1088Ser missense NM_001407749.1:c.3262C>T NP_001394678.1:p.Pro1088Ser missense NM_001407750.1:c.3265C>T NP_001394679.1:p.Pro1089Ser missense NM_001407751.1:c.3265C>T NP_001394680.1:p.Pro1089Ser missense NM_001407752.1:c.3265C>T NP_001394681.1:p.Pro1089Ser missense NM_001407838.1:c.3262C>T NP_001394767.1:p.Pro1088Ser missense NM_001407839.1:c.3262C>T NP_001394768.1:p.Pro1088Ser missense NM_001407841.1:c.3262C>T NP_001394770.1:p.Pro1088Ser missense NM_001407842.1:c.3262C>T NP_001394771.1:p.Pro1088Ser missense NM_001407843.1:c.3262C>T NP_001394772.1:p.Pro1088Ser missense NM_001407844.1:c.3262C>T NP_001394773.1:p.Pro1088Ser missense NM_001407845.1:c.3262C>T NP_001394774.1:p.Pro1088Ser missense NM_001407846.1:c.3262C>T NP_001394775.1:p.Pro1088Ser missense NM_001407847.1:c.3262C>T NP_001394776.1:p.Pro1088Ser missense NM_001407848.1:c.3262C>T NP_001394777.1:p.Pro1088Ser missense NM_001407849.1:c.3262C>T NP_001394778.1:p.Pro1088Ser missense NM_001407850.1:c.3265C>T NP_001394779.1:p.Pro1089Ser missense NM_001407851.1:c.3265C>T NP_001394780.1:p.Pro1089Ser missense NM_001407852.1:c.3265C>T NP_001394781.1:p.Pro1089Ser missense NM_001407853.1:c.3193C>T NP_001394782.1:p.Pro1065Ser missense NM_001407854.1:c.3406C>T NP_001394783.1:p.Pro1136Ser missense NM_001407858.1:c.3406C>T NP_001394787.1:p.Pro1136Ser missense NM_001407859.1:c.3406C>T NP_001394788.1:p.Pro1136Ser missense NM_001407860.1:c.3403C>T NP_001394789.1:p.Pro1135Ser missense NM_001407861.1:c.3403C>T NP_001394790.1:p.Pro1135Ser missense NM_001407862.1:c.3205C>T NP_001394791.1:p.Pro1069Ser missense NM_001407863.1:c.3283C>T NP_001394792.1:p.Pro1095Ser missense NM_001407874.1:c.3202C>T NP_001394803.1:p.Pro1068Ser missense NM_001407875.1:c.3202C>T NP_001394804.1:p.Pro1068Ser missense NM_001407879.1:c.3196C>T NP_001394808.1:p.Pro1066Ser missense NM_001407881.1:c.3196C>T NP_001394810.1:p.Pro1066Ser missense NM_001407882.1:c.3196C>T NP_001394811.1:p.Pro1066Ser missense NM_001407884.1:c.3196C>T NP_001394813.1:p.Pro1066Ser missense NM_001407885.1:c.3196C>T NP_001394814.1:p.Pro1066Ser missense NM_001407886.1:c.3196C>T NP_001394815.1:p.Pro1066Ser missense NM_001407887.1:c.3196C>T NP_001394816.1:p.Pro1066Ser missense NM_001407889.1:c.3196C>T NP_001394818.1:p.Pro1066Ser missense NM_001407894.1:c.3193C>T NP_001394823.1:p.Pro1065Ser missense NM_001407895.1:c.3193C>T NP_001394824.1:p.Pro1065Ser missense NM_001407896.1:c.3193C>T NP_001394825.1:p.Pro1065Ser missense NM_001407897.1:c.3193C>T NP_001394826.1:p.Pro1065Ser missense NM_001407898.1:c.3193C>T NP_001394827.1:p.Pro1065Ser missense NM_001407899.1:c.3193C>T NP_001394828.1:p.Pro1065Ser missense NM_001407900.1:c.3196C>T NP_001394829.1:p.Pro1066Ser missense NM_001407902.1:c.3196C>T NP_001394831.1:p.Pro1066Ser missense NM_001407904.1:c.3196C>T NP_001394833.1:p.Pro1066Ser missense NM_001407906.1:c.3196C>T NP_001394835.1:p.Pro1066Ser missense NM_001407907.1:c.3196C>T NP_001394836.1:p.Pro1066Ser missense NM_001407908.1:c.3196C>T NP_001394837.1:p.Pro1066Ser missense NM_001407909.1:c.3196C>T NP_001394838.1:p.Pro1066Ser missense NM_001407910.1:c.3196C>T NP_001394839.1:p.Pro1066Ser missense NM_001407915.1:c.3193C>T NP_001394844.1:p.Pro1065Ser missense NM_001407916.1:c.3193C>T NP_001394845.1:p.Pro1065Ser missense NM_001407917.1:c.3193C>T NP_001394846.1:p.Pro1065Ser missense NM_001407918.1:c.3193C>T NP_001394847.1:p.Pro1065Ser missense NM_001407919.1:c.3283C>T NP_001394848.1:p.Pro1095Ser missense NM_001407920.1:c.3142C>T NP_001394849.1:p.Pro1048Ser missense NM_001407921.1:c.3142C>T NP_001394850.1:p.Pro1048Ser missense NM_001407922.1:c.3142C>T NP_001394851.1:p.Pro1048Ser missense NM_001407923.1:c.3142C>T NP_001394852.1:p.Pro1048Ser missense NM_001407924.1:c.3142C>T NP_001394853.1:p.Pro1048Ser missense NM_001407925.1:c.3142C>T NP_001394854.1:p.Pro1048Ser missense NM_001407926.1:c.3142C>T NP_001394855.1:p.Pro1048Ser missense NM_001407927.1:c.3142C>T NP_001394856.1:p.Pro1048Ser missense NM_001407928.1:c.3142C>T NP_001394857.1:p.Pro1048Ser missense NM_001407929.1:c.3142C>T NP_001394858.1:p.Pro1048Ser missense NM_001407930.1:c.3139C>T NP_001394859.1:p.Pro1047Ser missense NM_001407931.1:c.3139C>T NP_001394860.1:p.Pro1047Ser missense NM_001407932.1:c.3139C>T NP_001394861.1:p.Pro1047Ser missense NM_001407933.1:c.3142C>T NP_001394862.1:p.Pro1048Ser missense NM_001407934.1:c.3139C>T NP_001394863.1:p.Pro1047Ser missense NM_001407935.1:c.3142C>T NP_001394864.1:p.Pro1048Ser missense NM_001407936.1:c.3139C>T NP_001394865.1:p.Pro1047Ser missense NM_001407937.1:c.3283C>T NP_001394866.1:p.Pro1095Ser missense NM_001407938.1:c.3283C>T NP_001394867.1:p.Pro1095Ser missense NM_001407939.1:c.3283C>T NP_001394868.1:p.Pro1095Ser missense NM_001407940.1:c.3280C>T NP_001394869.1:p.Pro1094Ser missense NM_001407941.1:c.3280C>T NP_001394870.1:p.Pro1094Ser missense NM_001407942.1:c.3265C>T NP_001394871.1:p.Pro1089Ser missense NM_001407943.1:c.3262C>T NP_001394872.1:p.Pro1088Ser missense NM_001407944.1:c.3265C>T NP_001394873.1:p.Pro1089Ser missense NM_001407945.1:c.3265C>T NP_001394874.1:p.Pro1089Ser missense NM_001407946.1:c.3073C>T NP_001394875.1:p.Pro1025Ser missense NM_001407947.1:c.3073C>T NP_001394876.1:p.Pro1025Ser missense NM_001407948.1:c.3073C>T NP_001394877.1:p.Pro1025Ser missense NM_001407949.1:c.3073C>T NP_001394878.1:p.Pro1025Ser missense NM_001407950.1:c.3073C>T NP_001394879.1:p.Pro1025Ser missense NM_001407951.1:c.3073C>T NP_001394880.1:p.Pro1025Ser missense NM_001407952.1:c.3073C>T NP_001394881.1:p.Pro1025Ser missense NM_001407953.1:c.3073C>T NP_001394882.1:p.Pro1025Ser missense NM_001407954.1:c.3070C>T NP_001394883.1:p.Pro1024Ser missense NM_001407955.1:c.3070C>T NP_001394884.1:p.Pro1024Ser missense NM_001407956.1:c.3070C>T NP_001394885.1:p.Pro1024Ser missense NM_001407957.1:c.3073C>T NP_001394886.1:p.Pro1025Ser missense NM_001407958.1:c.3070C>T NP_001394887.1:p.Pro1024Ser missense NM_001407959.1:c.3025C>T NP_001394888.1:p.Pro1009Ser missense NM_001407960.1:c.3025C>T NP_001394889.1:p.Pro1009Ser missense NM_001407962.1:c.3022C>T NP_001394891.1:p.Pro1008Ser missense NM_001407963.1:c.3025C>T NP_001394892.1:p.Pro1009Ser missense NM_001407964.1:c.3262C>T NP_001394893.1:p.Pro1088Ser missense NM_001407965.1:c.2902C>T NP_001394894.1:p.Pro968Ser missense NM_001407966.1:c.2518C>T NP_001394895.1:p.Pro840Ser missense NM_001407967.1:c.2518C>T NP_001394896.1:p.Pro840Ser missense NM_001407968.1:c.802C>T NP_001394897.1:p.Pro268Ser missense NM_001407969.1:c.802C>T NP_001394898.1:p.Pro268Ser missense NM_001407970.1:c.788-1093C>T intron variant NM_001407971.1:c.788-1093C>T intron variant NM_001407972.1:c.785-1093C>T intron variant NM_001407973.1:c.788-1093C>T intron variant NM_001407974.1:c.788-1093C>T intron variant NM_001407975.1:c.788-1093C>T intron variant NM_001407976.1:c.788-1093C>T intron variant NM_001407977.1:c.788-1093C>T intron variant NM_001407978.1:c.788-1093C>T intron variant NM_001407979.1:c.788-1093C>T intron variant NM_001407980.1:c.788-1093C>T intron variant NM_001407981.1:c.788-1093C>T intron variant NM_001407982.1:c.788-1093C>T intron variant NM_001407983.1:c.788-1093C>T intron variant NM_001407984.1:c.785-1093C>T intron variant NM_001407985.1:c.785-1093C>T intron variant NM_001407986.1:c.785-1093C>T intron variant NM_001407990.1:c.788-1093C>T intron variant NM_001407991.1:c.785-1093C>T intron variant NM_001407992.1:c.785-1093C>T intron variant NM_001407993.1:c.788-1093C>T intron variant NM_001408392.1:c.785-1093C>T intron variant NM_001408396.1:c.785-1093C>T intron variant NM_001408397.1:c.785-1093C>T intron variant NM_001408398.1:c.785-1093C>T intron variant NM_001408399.1:c.785-1093C>T intron variant NM_001408400.1:c.785-1093C>T intron variant NM_001408401.1:c.785-1093C>T intron variant NM_001408402.1:c.785-1093C>T intron variant NM_001408403.1:c.788-1093C>T intron variant NM_001408404.1:c.788-1093C>T intron variant NM_001408406.1:c.791-1102C>T intron variant NM_001408407.1:c.785-1093C>T intron variant NM_001408408.1:c.779-1093C>T intron variant NM_001408409.1:c.710-1093C>T intron variant NM_001408410.1:c.647-1093C>T intron variant NM_001408411.1:c.710-1093C>T intron variant NM_001408412.1:c.710-1093C>T intron variant NM_001408413.1:c.707-1093C>T intron variant NM_001408414.1:c.710-1093C>T intron variant NM_001408415.1:c.710-1093C>T intron variant NM_001408416.1:c.707-1093C>T intron variant NM_001408418.1:c.671-1093C>T intron variant NM_001408419.1:c.671-1093C>T intron variant NM_001408420.1:c.671-1093C>T intron variant NM_001408421.1:c.668-1093C>T intron variant NM_001408422.1:c.671-1093C>T intron variant NM_001408423.1:c.671-1093C>T intron variant NM_001408424.1:c.668-1093C>T intron variant NM_001408425.1:c.665-1093C>T intron variant NM_001408426.1:c.665-1093C>T intron variant NM_001408427.1:c.665-1093C>T intron variant NM_001408428.1:c.665-1093C>T intron variant NM_001408429.1:c.665-1093C>T intron variant NM_001408430.1:c.665-1093C>T intron variant NM_001408431.1:c.668-1093C>T intron variant NM_001408432.1:c.662-1093C>T intron variant NM_001408433.1:c.662-1093C>T intron variant NM_001408434.1:c.662-1093C>T intron variant NM_001408435.1:c.662-1093C>T intron variant NM_001408436.1:c.665-1093C>T intron variant NM_001408437.1:c.665-1093C>T intron variant NM_001408438.1:c.665-1093C>T intron variant NM_001408439.1:c.665-1093C>T intron variant NM_001408440.1:c.665-1093C>T intron variant NM_001408441.1:c.665-1093C>T intron variant NM_001408442.1:c.665-1093C>T intron variant NM_001408443.1:c.665-1093C>T intron variant NM_001408444.1:c.665-1093C>T intron variant NM_001408445.1:c.662-1093C>T intron variant NM_001408446.1:c.662-1093C>T intron variant NM_001408447.1:c.662-1093C>T intron variant NM_001408448.1:c.662-1093C>T intron variant NM_001408450.1:c.662-1093C>T intron variant NM_001408451.1:c.653-1093C>T intron variant NM_001408452.1:c.647-1093C>T intron variant NM_001408453.1:c.647-1093C>T intron variant NM_001408454.1:c.647-1093C>T intron variant NM_001408455.1:c.647-1093C>T intron variant NM_001408456.1:c.647-1093C>T intron variant NM_001408457.1:c.647-1093C>T intron variant NM_001408458.1:c.647-1093C>T intron variant NM_001408459.1:c.647-1093C>T intron variant NM_001408460.1:c.647-1093C>T intron variant NM_001408461.1:c.647-1093C>T intron variant NM_001408462.1:c.644-1093C>T intron variant NM_001408463.1:c.644-1093C>T intron variant NM_001408464.1:c.644-1093C>T intron variant NM_001408465.1:c.644-1093C>T intron variant NM_001408466.1:c.647-1093C>T intron variant NM_001408467.1:c.647-1093C>T intron variant NM_001408468.1:c.644-1093C>T intron variant NM_001408469.1:c.647-1093C>T intron variant NM_001408470.1:c.644-1093C>T intron variant NM_001408472.1:c.788-1093C>T intron variant NM_001408473.1:c.785-1093C>T intron variant NM_001408474.1:c.587-1093C>T intron variant NM_001408475.1:c.584-1093C>T intron variant NM_001408476.1:c.587-1093C>T intron variant NM_001408478.1:c.578-1093C>T intron variant NM_001408479.1:c.578-1093C>T intron variant NM_001408480.1:c.578-1093C>T intron variant NM_001408481.1:c.578-1093C>T intron variant NM_001408482.1:c.578-1093C>T intron variant NM_001408483.1:c.578-1093C>T intron variant NM_001408484.1:c.578-1093C>T intron variant NM_001408485.1:c.578-1093C>T intron variant NM_001408489.1:c.578-1093C>T intron variant NM_001408490.1:c.575-1093C>T intron variant NM_001408491.1:c.575-1093C>T intron variant NM_001408492.1:c.578-1093C>T intron variant NM_001408493.1:c.575-1093C>T intron variant NM_001408494.1:c.548-1093C>T intron variant NM_001408495.1:c.545-1093C>T intron variant NM_001408496.1:c.524-1093C>T intron variant NM_001408497.1:c.524-1093C>T intron variant NM_001408498.1:c.524-1093C>T intron variant NM_001408499.1:c.524-1093C>T intron variant NM_001408500.1:c.524-1093C>T intron variant NM_001408501.1:c.524-1093C>T intron variant NM_001408502.1:c.455-1093C>T intron variant NM_001408503.1:c.521-1093C>T intron variant NM_001408504.1:c.521-1093C>T intron variant NM_001408505.1:c.521-1093C>T intron variant NM_001408506.1:c.461-1093C>T intron variant NM_001408507.1:c.461-1093C>T intron variant NM_001408508.1:c.452-1093C>T intron variant NM_001408509.1:c.452-1093C>T intron variant NM_001408510.1:c.407-1093C>T intron variant NM_001408511.1:c.404-1093C>T intron variant NM_001408512.1:c.284-1093C>T intron variant NM_001408513.1:c.578-1093C>T intron variant NM_001408514.1:c.578-1093C>T intron variant NM_007297.4:c.3265C>T NP_009228.2:p.Pro1089Ser missense NM_007298.4:c.788-1093C>T intron variant NM_007299.4:c.788-1093C>T intron variant NM_007300.4:c.3406C>T NP_009231.2:p.Pro1136Ser missense NR_027676.1:n.3542C>T NC_000017.11:g.43092125G>A NC_000017.10:g.41244142G>A NG_005905.2:g.125859C>T NG_087068.1:g.1107G>A LRG_292:g.125859C>T LRG_292t1:c.3406C>T LRG_292p1:p.Pro1136Ser - Protein change
- P1089S, P1136S, P840S, P1047S, P1109S, P1008S, P1025S, P1065S, P1069S, P1088S, P1110S, P968S, P1009S, P1024S, P1048S, P1066S, P1068S, P1094S, P1095S, P1133S, P1135S, P268S
- Other names
- -
- Canonical SPDI
- NC_000017.11:43092124:G:A
-
Functional
consequence HelpThe effect of the variant on RNA or protein function, based on experimental evidence from submitters.
-
-
Global minor allele
frequency (GMAF) HelpThe global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.
-
-
Allele frequency
Help
The frequency of the allele represented by this VCV record.
Exome Aggregation Consortium (ExAC) 0.00001
- Links
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation |
Variation Viewer
Help
Links to Variation Viewer, a genome browser to view variation data from NCBI databases. |
Related variants | ||
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HI score
Help
The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team. |
TS score
Help
The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team. |
Within gene
Help
The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants. |
All
Help
The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene. |
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BRCA1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
13037 | 14843 | |
LOC126862571 | - | - | - | GRCh38 | - | 1651 |
Conditions - Germline
Condition
Help
The condition for this variant-condition (RCV) record in ClinVar. |
Classification
Help
The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions) |
Review status
Help
The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. |
Last evaluated
Help
The most recent date that a submitter evaluated this variant for the condition. |
Variation/condition record
Help
The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page. |
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Conflicting interpretations of pathogenicity (3) |
criteria provided, conflicting classifications
|
Mar 23, 2023 | RCV001020222.11 | |
Uncertain significance (1) |
criteria provided, single submitter
|
Dec 6, 2022 | RCV001860975.5 | |
Uncertain significance (1) |
criteria provided, single submitter
|
Dec 10, 2022 | RCV003233926.1 |
Submissions - Germline
Classification
Help
The submitted germline classification for each SCV record. (Last evaluated) |
Review status
Help
Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria) |
Condition
Help
The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant. |
Submitter
Help
The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar. |
More information
Help
This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter. |
|
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Likely benign
(Mar 23, 2023)
|
criteria provided, single submitter
Method: curation
|
Hereditary cancer-predisposing syndrome
Affected status: unknown
Allele origin:
germline
|
University of Washington Department of Laboratory Medicine, University of Washington
Accession: SCV003850424.1
First in ClinVar: Apr 01, 2023 Last updated: Apr 01, 2023
Comment:
BRCA1 coldspot (exon 11 using historical exon numbering). Reclassification based on statistical prior probability
|
Comment:
Missense variant in a coldspot region where missense variants are very unlikely to be pathogenic (PMID:31911673).
|
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Uncertain significance
(Dec 10, 2022)
|
criteria provided, single submitter
Method: clinical testing
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Not Provided
Affected status: yes
Allele origin:
germline
|
GeneDx
Accession: SCV003931122.1
First in ClinVar: Jun 17, 2023 Last updated: Jun 17, 2023 |
Comment:
Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; … (more)
Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; Also known as 3525C>T; This variant is associated with the following publications: (PMID: 32377563, 29884841) (less)
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Uncertain significance
(May 29, 2019)
|
criteria provided, single submitter
Method: clinical testing
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Hereditary cancer-predisposing syndrome
Affected status: unknown
Allele origin:
germline
|
Ambry Genetics
Accession: SCV001181673.4
First in ClinVar: Mar 16, 2020 Last updated: May 01, 2024 |
Comment:
The p.P1136S variant (also known as c.3406C>T), located in coding exon 9 of the BRCA1 gene, results from a C to T substitution at nucleotide … (more)
The p.P1136S variant (also known as c.3406C>T), located in coding exon 9 of the BRCA1 gene, results from a C to T substitution at nucleotide position 3406. The proline at codon 1136 is replaced by serine, an amino acid with similar properties. This amino acid position is not well conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. (less)
|
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Uncertain significance
(Feb 14, 2020)
|
criteria provided, single submitter
Method: clinical testing
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Hereditary cancer-predisposing syndrome
Affected status: unknown
Allele origin:
germline
|
Color Diagnostics, LLC DBA Color Health
Accession: SCV001348541.2
First in ClinVar: Jun 22, 2020 Last updated: Jan 12, 2022 |
Comment:
This missense variant replaces proline with serine at codon 1136 of the BRCA1 protein. Computational prediction suggests that this variant may not impact protein structure … (more)
This missense variant replaces proline with serine at codon 1136 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). Splice site prediction tools suggest that this variant may not impact RNA splicing. To our knowledge, functional studies have not been performed for this variant. This variant has not been reported in individuals affected with hereditary cancer in the literature. This variant has been identified in 1/250892 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. (less)
|
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Uncertain significance
(Dec 06, 2022)
|
criteria provided, single submitter
Method: clinical testing
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Hereditary breast ovarian cancer syndrome
Affected status: unknown
Allele origin:
germline
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Labcorp Genetics (formerly Invitae), Labcorp
Accession: SCV002122606.3
First in ClinVar: Mar 28, 2022 Last updated: Feb 28, 2024 |
Comment:
ClinVar contains an entry for this variant (Variation ID: 823737). This variant has not been reported in the literature in individuals affected with BRCA1-related conditions. … (more)
ClinVar contains an entry for this variant (Variation ID: 823737). This variant has not been reported in the literature in individuals affected with BRCA1-related conditions. This variant is present in population databases (rs431825395, gnomAD 0.003%). This sequence change replaces proline, which is neutral and non-polar, with serine, which is neutral and polar, at codon 1136 of the BRCA1 protein (p.Pro1136Ser). 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. 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. (less)
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Germline Functional Evidence
There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar. |
Citations for germline classification of this variant
HelpTitle | Author | Journal | Year | Link |
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Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots". | Dines JN | Genetics in medicine : official journal of the American College of Medical Genetics | 2020 | PMID: 31911673 |
Text-mined citations for rs431825395 ...
HelpRecord last updated Sep 29, 2024
This date represents the last time this VCV record was updated. The update may be due to an update to one of the included submitted records (SCVs), or due to an update that ClinVar made to the variant such as adding HGVS expressions or a rs number. So this date may be different from the date of the “most recent submission” reported at the top of this page.