ClinVar Genomic variation as it relates to human health
NM_007294.4(BRCA1):c.1664A>G (p.Asn555Ser)
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(2); Likely benign(1)
No data submitted for somatic clinical impact
No data submitted for oncogenicity
Variant Details
- Identifiers
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NM_007294.4(BRCA1):c.1664A>G (p.Asn555Ser)
Variation ID: 1489883 Accession: VCV001489883.11
- Type and length
-
single nucleotide variant, 1 bp
- Location
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Cytogenetic: 17q21.31 17: 43093867 (GRCh38) [ NCBI UCSC ] 17: 41245884 (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 28, 2022 May 1, 2024 Mar 23, 2023 - HGVS
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Nucleotide Protein Molecular
consequenceNM_007294.4:c.1664A>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_009225.1:p.Asn555Ser missense NM_001407571.1:c.1451A>G NP_001394500.1:p.Asn484Ser missense NM_001407581.1:c.1664A>G NP_001394510.1:p.Asn555Ser missense NM_001407582.1:c.1664A>G NP_001394511.1:p.Asn555Ser missense NM_001407583.1:c.1664A>G NP_001394512.1:p.Asn555Ser missense NM_001407585.1:c.1664A>G NP_001394514.1:p.Asn555Ser missense NM_001407587.1:c.1661A>G NP_001394516.1:p.Asn554Ser missense NM_001407590.1:c.1661A>G NP_001394519.1:p.Asn554Ser missense NM_001407591.1:c.1661A>G NP_001394520.1:p.Asn554Ser missense NM_001407593.1:c.1664A>G NP_001394522.1:p.Asn555Ser missense NM_001407594.1:c.1664A>G NP_001394523.1:p.Asn555Ser missense NM_001407596.1:c.1664A>G NP_001394525.1:p.Asn555Ser missense NM_001407597.1:c.1664A>G NP_001394526.1:p.Asn555Ser missense NM_001407598.1:c.1664A>G NP_001394527.1:p.Asn555Ser missense NM_001407602.1:c.1664A>G NP_001394531.1:p.Asn555Ser missense NM_001407603.1:c.1664A>G NP_001394532.1:p.Asn555Ser missense NM_001407605.1:c.1664A>G NP_001394534.1:p.Asn555Ser missense NM_001407610.1:c.1661A>G NP_001394539.1:p.Asn554Ser missense NM_001407611.1:c.1661A>G NP_001394540.1:p.Asn554Ser missense NM_001407612.1:c.1661A>G NP_001394541.1:p.Asn554Ser missense NM_001407613.1:c.1661A>G NP_001394542.1:p.Asn554Ser missense NM_001407614.1:c.1661A>G NP_001394543.1:p.Asn554Ser missense NM_001407615.1:c.1661A>G NP_001394544.1:p.Asn554Ser missense NM_001407616.1:c.1664A>G NP_001394545.1:p.Asn555Ser missense NM_001407617.1:c.1664A>G NP_001394546.1:p.Asn555Ser missense NM_001407618.1:c.1664A>G NP_001394547.1:p.Asn555Ser missense NM_001407619.1:c.1664A>G NP_001394548.1:p.Asn555Ser missense NM_001407620.1:c.1664A>G NP_001394549.1:p.Asn555Ser missense NM_001407621.1:c.1664A>G NP_001394550.1:p.Asn555Ser missense NM_001407622.1:c.1664A>G NP_001394551.1:p.Asn555Ser missense NM_001407623.1:c.1664A>G NP_001394552.1:p.Asn555Ser missense NM_001407624.1:c.1664A>G NP_001394553.1:p.Asn555Ser missense NM_001407625.1:c.1664A>G NP_001394554.1:p.Asn555Ser missense NM_001407626.1:c.1664A>G NP_001394555.1:p.Asn555Ser missense NM_001407627.1:c.1661A>G NP_001394556.1:p.Asn554Ser missense NM_001407628.1:c.1661A>G NP_001394557.1:p.Asn554Ser missense NM_001407629.1:c.1661A>G NP_001394558.1:p.Asn554Ser missense NM_001407630.1:c.1661A>G NP_001394559.1:p.Asn554Ser missense NM_001407631.1:c.1661A>G NP_001394560.1:p.Asn554Ser missense NM_001407632.1:c.1661A>G NP_001394561.1:p.Asn554Ser missense NM_001407633.1:c.1661A>G NP_001394562.1:p.Asn554Ser missense NM_001407634.1:c.1661A>G NP_001394563.1:p.Asn554Ser missense NM_001407635.1:c.1661A>G NP_001394564.1:p.Asn554Ser missense NM_001407636.1:c.1661A>G NP_001394565.1:p.Asn554Ser missense NM_001407637.1:c.1661A>G NP_001394566.1:p.Asn554Ser missense NM_001407638.1:c.1661A>G NP_001394567.1:p.Asn554Ser missense NM_001407639.1:c.1664A>G NP_001394568.1:p.Asn555Ser missense NM_001407640.1:c.1664A>G NP_001394569.1:p.Asn555Ser missense NM_001407641.1:c.1664A>G NP_001394570.1:p.Asn555Ser missense NM_001407642.1:c.1664A>G NP_001394571.1:p.Asn555Ser missense NM_001407644.1:c.1661A>G NP_001394573.1:p.Asn554Ser missense NM_001407645.1:c.1661A>G NP_001394574.1:p.Asn554Ser missense NM_001407646.1:c.1655A>G NP_001394575.1:p.Asn552Ser missense NM_001407647.1:c.1655A>G NP_001394576.1:p.Asn552Ser missense NM_001407648.1:c.1541A>G NP_001394577.1:p.Asn514Ser missense NM_001407649.1:c.1538A>G NP_001394578.1:p.Asn513Ser missense NM_001407652.1:c.1664A>G NP_001394581.1:p.Asn555Ser missense NM_001407653.1:c.1586A>G NP_001394582.1:p.Asn529Ser missense NM_001407654.1:c.1586A>G NP_001394583.1:p.Asn529Ser missense NM_001407655.1:c.1586A>G NP_001394584.1:p.Asn529Ser missense NM_001407656.1:c.1586A>G NP_001394585.1:p.Asn529Ser missense NM_001407657.1:c.1586A>G NP_001394586.1:p.Asn529Ser missense NM_001407658.1:c.1586A>G NP_001394587.1:p.Asn529Ser missense NM_001407659.1:c.1583A>G NP_001394588.1:p.Asn528Ser missense NM_001407660.1:c.1583A>G NP_001394589.1:p.Asn528Ser missense NM_001407661.1:c.1583A>G NP_001394590.1:p.Asn528Ser missense NM_001407662.1:c.1583A>G NP_001394591.1:p.Asn528Ser missense NM_001407663.1:c.1586A>G NP_001394592.1:p.Asn529Ser missense NM_001407664.1:c.1541A>G NP_001394593.1:p.Asn514Ser missense NM_001407665.1:c.1541A>G NP_001394594.1:p.Asn514Ser missense NM_001407666.1:c.1541A>G NP_001394595.1:p.Asn514Ser missense NM_001407667.1:c.1541A>G NP_001394596.1:p.Asn514Ser missense NM_001407668.1:c.1541A>G NP_001394597.1:p.Asn514Ser missense NM_001407669.1:c.1541A>G NP_001394598.1:p.Asn514Ser missense NM_001407670.1:c.1538A>G NP_001394599.1:p.Asn513Ser missense NM_001407671.1:c.1538A>G NP_001394600.1:p.Asn513Ser missense NM_001407672.1:c.1538A>G NP_001394601.1:p.Asn513Ser missense NM_001407673.1:c.1538A>G NP_001394602.1:p.Asn513Ser missense NM_001407674.1:c.1541A>G NP_001394603.1:p.Asn514Ser missense NM_001407675.1:c.1541A>G NP_001394604.1:p.Asn514Ser missense NM_001407676.1:c.1541A>G NP_001394605.1:p.Asn514Ser missense NM_001407677.1:c.1541A>G NP_001394606.1:p.Asn514Ser missense NM_001407678.1:c.1541A>G NP_001394607.1:p.Asn514Ser missense NM_001407679.1:c.1541A>G NP_001394608.1:p.Asn514Ser missense NM_001407680.1:c.1541A>G NP_001394609.1:p.Asn514Ser missense NM_001407681.1:c.1541A>G NP_001394610.1:p.Asn514Ser missense NM_001407682.1:c.1541A>G NP_001394611.1:p.Asn514Ser missense NM_001407683.1:c.1541A>G NP_001394612.1:p.Asn514Ser missense NM_001407684.1:c.1664A>G NP_001394613.1:p.Asn555Ser missense NM_001407685.1:c.1538A>G NP_001394614.1:p.Asn513Ser missense NM_001407686.1:c.1538A>G NP_001394615.1:p.Asn513Ser missense NM_001407687.1:c.1538A>G NP_001394616.1:p.Asn513Ser missense NM_001407688.1:c.1538A>G NP_001394617.1:p.Asn513Ser missense NM_001407689.1:c.1538A>G NP_001394618.1:p.Asn513Ser missense NM_001407690.1:c.1538A>G NP_001394619.1:p.Asn513Ser missense NM_001407691.1:c.1538A>G NP_001394620.1:p.Asn513Ser missense NM_001407692.1:c.1523A>G NP_001394621.1:p.Asn508Ser missense NM_001407694.1:c.1523A>G NP_001394623.1:p.Asn508Ser missense NM_001407695.1:c.1523A>G NP_001394624.1:p.Asn508Ser missense NM_001407696.1:c.1523A>G NP_001394625.1:p.Asn508Ser missense NM_001407697.1:c.1523A>G NP_001394626.1:p.Asn508Ser missense NM_001407698.1:c.1523A>G NP_001394627.1:p.Asn508Ser missense NM_001407724.1:c.1523A>G NP_001394653.1:p.Asn508Ser missense NM_001407725.1:c.1523A>G NP_001394654.1:p.Asn508Ser missense NM_001407726.1:c.1523A>G NP_001394655.1:p.Asn508Ser missense NM_001407727.1:c.1523A>G NP_001394656.1:p.Asn508Ser missense NM_001407728.1:c.1523A>G NP_001394657.1:p.Asn508Ser missense NM_001407729.1:c.1523A>G NP_001394658.1:p.Asn508Ser missense NM_001407730.1:c.1523A>G NP_001394659.1:p.Asn508Ser missense NM_001407731.1:c.1523A>G NP_001394660.1:p.Asn508Ser missense NM_001407732.1:c.1523A>G NP_001394661.1:p.Asn508Ser missense NM_001407733.1:c.1523A>G NP_001394662.1:p.Asn508Ser missense NM_001407734.1:c.1523A>G NP_001394663.1:p.Asn508Ser missense NM_001407735.1:c.1523A>G NP_001394664.1:p.Asn508Ser missense NM_001407736.1:c.1523A>G NP_001394665.1:p.Asn508Ser missense NM_001407737.1:c.1523A>G NP_001394666.1:p.Asn508Ser missense NM_001407738.1:c.1523A>G NP_001394667.1:p.Asn508Ser missense NM_001407739.1:c.1523A>G NP_001394668.1:p.Asn508Ser missense NM_001407740.1:c.1520A>G NP_001394669.1:p.Asn507Ser missense NM_001407741.1:c.1520A>G NP_001394670.1:p.Asn507Ser missense NM_001407742.1:c.1520A>G NP_001394671.1:p.Asn507Ser missense NM_001407743.1:c.1520A>G NP_001394672.1:p.Asn507Ser missense NM_001407744.1:c.1520A>G NP_001394673.1:p.Asn507Ser missense NM_001407745.1:c.1520A>G NP_001394674.1:p.Asn507Ser missense NM_001407746.1:c.1520A>G NP_001394675.1:p.Asn507Ser missense NM_001407747.1:c.1520A>G NP_001394676.1:p.Asn507Ser missense NM_001407748.1:c.1520A>G NP_001394677.1:p.Asn507Ser missense NM_001407749.1:c.1520A>G NP_001394678.1:p.Asn507Ser missense NM_001407750.1:c.1523A>G NP_001394679.1:p.Asn508Ser missense NM_001407751.1:c.1523A>G NP_001394680.1:p.Asn508Ser missense NM_001407752.1:c.1523A>G NP_001394681.1:p.Asn508Ser missense NM_001407838.1:c.1520A>G NP_001394767.1:p.Asn507Ser missense NM_001407839.1:c.1520A>G NP_001394768.1:p.Asn507Ser missense NM_001407841.1:c.1520A>G NP_001394770.1:p.Asn507Ser missense NM_001407842.1:c.1520A>G NP_001394771.1:p.Asn507Ser missense NM_001407843.1:c.1520A>G NP_001394772.1:p.Asn507Ser missense NM_001407844.1:c.1520A>G NP_001394773.1:p.Asn507Ser missense NM_001407845.1:c.1520A>G NP_001394774.1:p.Asn507Ser missense NM_001407846.1:c.1520A>G NP_001394775.1:p.Asn507Ser missense NM_001407847.1:c.1520A>G NP_001394776.1:p.Asn507Ser missense NM_001407848.1:c.1520A>G NP_001394777.1:p.Asn507Ser missense NM_001407849.1:c.1520A>G NP_001394778.1:p.Asn507Ser missense NM_001407850.1:c.1523A>G NP_001394779.1:p.Asn508Ser missense NM_001407851.1:c.1523A>G NP_001394780.1:p.Asn508Ser missense NM_001407852.1:c.1523A>G NP_001394781.1:p.Asn508Ser missense NM_001407853.1:c.1451A>G NP_001394782.1:p.Asn484Ser missense NM_001407854.1:c.1664A>G NP_001394783.1:p.Asn555Ser missense NM_001407858.1:c.1664A>G NP_001394787.1:p.Asn555Ser missense NM_001407859.1:c.1664A>G NP_001394788.1:p.Asn555Ser missense NM_001407860.1:c.1661A>G NP_001394789.1:p.Asn554Ser missense NM_001407861.1:c.1661A>G NP_001394790.1:p.Asn554Ser missense NM_001407862.1:c.1463A>G NP_001394791.1:p.Asn488Ser missense NM_001407863.1:c.1541A>G NP_001394792.1:p.Asn514Ser missense NM_001407874.1:c.1460A>G NP_001394803.1:p.Asn487Ser missense NM_001407875.1:c.1460A>G NP_001394804.1:p.Asn487Ser missense NM_001407879.1:c.1454A>G NP_001394808.1:p.Asn485Ser missense NM_001407881.1:c.1454A>G NP_001394810.1:p.Asn485Ser missense NM_001407882.1:c.1454A>G NP_001394811.1:p.Asn485Ser missense NM_001407884.1:c.1454A>G NP_001394813.1:p.Asn485Ser missense NM_001407885.1:c.1454A>G NP_001394814.1:p.Asn485Ser missense NM_001407886.1:c.1454A>G NP_001394815.1:p.Asn485Ser missense NM_001407887.1:c.1454A>G NP_001394816.1:p.Asn485Ser missense NM_001407889.1:c.1454A>G NP_001394818.1:p.Asn485Ser missense NM_001407894.1:c.1451A>G NP_001394823.1:p.Asn484Ser missense NM_001407895.1:c.1451A>G NP_001394824.1:p.Asn484Ser missense NM_001407896.1:c.1451A>G NP_001394825.1:p.Asn484Ser missense NM_001407897.1:c.1451A>G NP_001394826.1:p.Asn484Ser missense NM_001407898.1:c.1451A>G NP_001394827.1:p.Asn484Ser missense NM_001407899.1:c.1451A>G NP_001394828.1:p.Asn484Ser missense NM_001407900.1:c.1454A>G NP_001394829.1:p.Asn485Ser missense NM_001407902.1:c.1454A>G NP_001394831.1:p.Asn485Ser missense NM_001407904.1:c.1454A>G NP_001394833.1:p.Asn485Ser missense NM_001407906.1:c.1454A>G NP_001394835.1:p.Asn485Ser missense NM_001407907.1:c.1454A>G NP_001394836.1:p.Asn485Ser missense NM_001407908.1:c.1454A>G NP_001394837.1:p.Asn485Ser missense NM_001407909.1:c.1454A>G NP_001394838.1:p.Asn485Ser missense NM_001407910.1:c.1454A>G NP_001394839.1:p.Asn485Ser missense NM_001407915.1:c.1451A>G NP_001394844.1:p.Asn484Ser missense NM_001407916.1:c.1451A>G NP_001394845.1:p.Asn484Ser missense NM_001407917.1:c.1451A>G NP_001394846.1:p.Asn484Ser missense NM_001407918.1:c.1451A>G NP_001394847.1:p.Asn484Ser missense NM_001407919.1:c.1541A>G NP_001394848.1:p.Asn514Ser missense NM_001407920.1:c.1400A>G NP_001394849.1:p.Asn467Ser missense NM_001407921.1:c.1400A>G NP_001394850.1:p.Asn467Ser missense NM_001407922.1:c.1400A>G NP_001394851.1:p.Asn467Ser missense NM_001407923.1:c.1400A>G NP_001394852.1:p.Asn467Ser missense NM_001407924.1:c.1400A>G NP_001394853.1:p.Asn467Ser missense NM_001407925.1:c.1400A>G NP_001394854.1:p.Asn467Ser missense NM_001407926.1:c.1400A>G NP_001394855.1:p.Asn467Ser missense NM_001407927.1:c.1400A>G NP_001394856.1:p.Asn467Ser missense NM_001407928.1:c.1400A>G NP_001394857.1:p.Asn467Ser missense NM_001407929.1:c.1400A>G NP_001394858.1:p.Asn467Ser missense NM_001407930.1:c.1397A>G NP_001394859.1:p.Asn466Ser missense NM_001407931.1:c.1397A>G NP_001394860.1:p.Asn466Ser missense NM_001407932.1:c.1397A>G NP_001394861.1:p.Asn466Ser missense NM_001407933.1:c.1400A>G NP_001394862.1:p.Asn467Ser missense NM_001407934.1:c.1397A>G NP_001394863.1:p.Asn466Ser missense NM_001407935.1:c.1400A>G NP_001394864.1:p.Asn467Ser missense NM_001407936.1:c.1397A>G NP_001394865.1:p.Asn466Ser missense NM_001407937.1:c.1541A>G NP_001394866.1:p.Asn514Ser missense NM_001407938.1:c.1541A>G NP_001394867.1:p.Asn514Ser missense NM_001407939.1:c.1541A>G NP_001394868.1:p.Asn514Ser missense NM_001407940.1:c.1538A>G NP_001394869.1:p.Asn513Ser missense NM_001407941.1:c.1538A>G NP_001394870.1:p.Asn513Ser missense NM_001407942.1:c.1523A>G NP_001394871.1:p.Asn508Ser missense NM_001407943.1:c.1520A>G NP_001394872.1:p.Asn507Ser missense NM_001407944.1:c.1523A>G NP_001394873.1:p.Asn508Ser missense NM_001407945.1:c.1523A>G NP_001394874.1:p.Asn508Ser missense NM_001407946.1:c.1331A>G NP_001394875.1:p.Asn444Ser missense NM_001407947.1:c.1331A>G NP_001394876.1:p.Asn444Ser missense NM_001407948.1:c.1331A>G NP_001394877.1:p.Asn444Ser missense NM_001407949.1:c.1331A>G NP_001394878.1:p.Asn444Ser missense NM_001407950.1:c.1331A>G NP_001394879.1:p.Asn444Ser missense NM_001407951.1:c.1331A>G NP_001394880.1:p.Asn444Ser missense NM_001407952.1:c.1331A>G NP_001394881.1:p.Asn444Ser missense NM_001407953.1:c.1331A>G NP_001394882.1:p.Asn444Ser missense NM_001407954.1:c.1328A>G NP_001394883.1:p.Asn443Ser missense NM_001407955.1:c.1328A>G NP_001394884.1:p.Asn443Ser missense NM_001407956.1:c.1328A>G NP_001394885.1:p.Asn443Ser missense NM_001407957.1:c.1331A>G NP_001394886.1:p.Asn444Ser missense NM_001407958.1:c.1328A>G NP_001394887.1:p.Asn443Ser missense NM_001407959.1:c.1283A>G NP_001394888.1:p.Asn428Ser missense NM_001407960.1:c.1283A>G NP_001394889.1:p.Asn428Ser missense NM_001407962.1:c.1280A>G NP_001394891.1:p.Asn427Ser missense NM_001407963.1:c.1283A>G NP_001394892.1:p.Asn428Ser missense NM_001407964.1:c.1520A>G NP_001394893.1:p.Asn507Ser missense NM_001407965.1:c.1160A>G NP_001394894.1:p.Asn387Ser missense NM_001407966.1:c.776A>G NP_001394895.1:p.Asn259Ser missense NM_001407967.1:c.776A>G NP_001394896.1:p.Asn259Ser missense NM_001407968.1:c.787+877A>G intron variant NM_001407969.1:c.787+877A>G intron variant NM_001407970.1:c.787+877A>G intron variant NM_001407971.1:c.787+877A>G intron variant NM_001407972.1:c.784+877A>G intron variant NM_001407973.1:c.787+877A>G intron variant NM_001407974.1:c.787+877A>G intron variant NM_001407975.1:c.787+877A>G intron variant NM_001407976.1:c.787+877A>G intron variant NM_001407977.1:c.787+877A>G intron variant NM_001407978.1:c.787+877A>G intron variant NM_001407979.1:c.787+877A>G intron variant NM_001407980.1:c.787+877A>G intron variant NM_001407981.1:c.787+877A>G intron variant NM_001407982.1:c.787+877A>G intron variant NM_001407983.1:c.787+877A>G intron variant NM_001407984.1:c.784+877A>G intron variant NM_001407985.1:c.784+877A>G intron variant NM_001407986.1:c.784+877A>G intron variant NM_001407990.1:c.787+877A>G intron variant NM_001407991.1:c.784+877A>G intron variant NM_001407992.1:c.784+877A>G intron variant NM_001407993.1:c.787+877A>G intron variant NM_001408392.1:c.784+877A>G intron variant NM_001408396.1:c.784+877A>G intron variant NM_001408397.1:c.784+877A>G intron variant NM_001408398.1:c.784+877A>G intron variant NM_001408399.1:c.784+877A>G intron variant NM_001408400.1:c.784+877A>G intron variant NM_001408401.1:c.784+877A>G intron variant NM_001408402.1:c.784+877A>G intron variant NM_001408403.1:c.787+877A>G intron variant NM_001408404.1:c.787+877A>G intron variant NM_001408406.1:c.790+874A>G intron variant NM_001408407.1:c.784+877A>G intron variant NM_001408408.1:c.778+877A>G intron variant NM_001408409.1:c.709+877A>G intron variant NM_001408410.1:c.646+877A>G intron variant NM_001408411.1:c.709+877A>G intron variant NM_001408412.1:c.709+877A>G intron variant NM_001408413.1:c.706+877A>G intron variant NM_001408414.1:c.709+877A>G intron variant NM_001408415.1:c.709+877A>G intron variant NM_001408416.1:c.706+877A>G intron variant NM_001408418.1:c.670+1979A>G intron variant NM_001408419.1:c.670+1979A>G intron variant NM_001408420.1:c.670+1979A>G intron variant NM_001408421.1:c.667+1979A>G intron variant NM_001408422.1:c.670+1979A>G intron variant NM_001408423.1:c.670+1979A>G intron variant NM_001408424.1:c.667+1979A>G intron variant NM_001408425.1:c.664+877A>G intron variant NM_001408426.1:c.664+877A>G intron variant NM_001408427.1:c.664+877A>G intron variant NM_001408428.1:c.664+877A>G intron variant NM_001408429.1:c.664+877A>G intron variant NM_001408430.1:c.664+877A>G intron variant NM_001408431.1:c.667+1979A>G intron variant NM_001408432.1:c.661+877A>G intron variant NM_001408433.1:c.661+877A>G intron variant NM_001408434.1:c.661+877A>G intron variant NM_001408435.1:c.661+877A>G intron variant NM_001408436.1:c.664+877A>G intron variant NM_001408437.1:c.664+877A>G intron variant NM_001408438.1:c.664+877A>G intron variant NM_001408439.1:c.664+877A>G intron variant NM_001408440.1:c.664+877A>G intron variant NM_001408441.1:c.664+877A>G intron variant NM_001408442.1:c.664+877A>G intron variant NM_001408443.1:c.664+877A>G intron variant NM_001408444.1:c.664+877A>G intron variant NM_001408445.1:c.661+877A>G intron variant NM_001408446.1:c.661+877A>G intron variant NM_001408447.1:c.661+877A>G intron variant NM_001408448.1:c.661+877A>G intron variant NM_001408450.1:c.661+877A>G intron variant NM_001408451.1:c.652+877A>G intron variant NM_001408452.1:c.646+877A>G intron variant NM_001408453.1:c.646+877A>G intron variant NM_001408454.1:c.646+877A>G intron variant NM_001408455.1:c.646+877A>G intron variant NM_001408456.1:c.646+877A>G intron variant NM_001408457.1:c.646+877A>G intron variant NM_001408458.1:c.646+877A>G intron variant NM_001408459.1:c.646+877A>G intron variant NM_001408460.1:c.646+877A>G intron variant NM_001408461.1:c.646+877A>G intron variant NM_001408462.1:c.643+877A>G intron variant NM_001408463.1:c.643+877A>G intron variant NM_001408464.1:c.643+877A>G intron variant NM_001408465.1:c.643+877A>G intron variant NM_001408466.1:c.646+877A>G intron variant NM_001408467.1:c.646+877A>G intron variant NM_001408468.1:c.643+877A>G intron variant NM_001408469.1:c.646+877A>G intron variant NM_001408470.1:c.643+877A>G intron variant NM_001408472.1:c.787+877A>G intron variant NM_001408473.1:c.784+877A>G intron variant NM_001408474.1:c.586+877A>G intron variant NM_001408475.1:c.583+877A>G intron variant NM_001408476.1:c.586+877A>G intron variant NM_001408478.1:c.577+877A>G intron variant NM_001408479.1:c.577+877A>G intron variant NM_001408480.1:c.577+877A>G intron variant NM_001408481.1:c.577+877A>G intron variant NM_001408482.1:c.577+877A>G intron variant NM_001408483.1:c.577+877A>G intron variant NM_001408484.1:c.577+877A>G intron variant NM_001408485.1:c.577+877A>G intron variant NM_001408489.1:c.577+877A>G intron variant NM_001408490.1:c.574+877A>G intron variant NM_001408491.1:c.574+877A>G intron variant NM_001408492.1:c.577+877A>G intron variant NM_001408493.1:c.574+877A>G intron variant NM_001408494.1:c.548-2835A>G intron variant NM_001408495.1:c.545-2835A>G intron variant NM_001408496.1:c.523+877A>G intron variant NM_001408497.1:c.523+877A>G intron variant NM_001408498.1:c.523+877A>G intron variant NM_001408499.1:c.523+877A>G intron variant NM_001408500.1:c.523+877A>G intron variant NM_001408501.1:c.523+877A>G intron variant NM_001408502.1:c.454+877A>G intron variant NM_001408503.1:c.520+877A>G intron variant NM_001408504.1:c.520+877A>G intron variant NM_001408505.1:c.520+877A>G intron variant NM_001408506.1:c.460+1979A>G intron variant NM_001408507.1:c.460+1979A>G intron variant NM_001408508.1:c.451+877A>G intron variant NM_001408509.1:c.451+877A>G intron variant NM_001408510.1:c.406+877A>G intron variant NM_001408511.1:c.404-2835A>G intron variant NM_001408512.1:c.283+877A>G intron variant NM_001408513.1:c.577+877A>G intron variant NM_001408514.1:c.577+877A>G intron variant NM_007297.4:c.1523A>G NP_009228.2:p.Asn508Ser missense NM_007298.4:c.787+877A>G intron variant NM_007299.4:c.787+877A>G intron variant NM_007300.4:c.1664A>G NP_009231.2:p.Asn555Ser missense NR_027676.1:n.1800A>G NC_000017.11:g.43093867T>C NC_000017.10:g.41245884T>C NG_005905.2:g.124117A>G LRG_292:g.124117A>G LRG_292t1:c.1664A>G LRG_292p1:p.Asn555Ser - Protein change
- N508S, N555S, N387S, N443S, N513S, N528S, N466S, N487S, N529S, N552S, N554S, N428S, N444S, N484S, N485S, N514S, N259S, N427S, N467S, N488S, N507S
- Other names
- -
- Canonical SPDI
- NC_000017.11:43093866:T:C
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Functional
consequence HelpThe effect of the variant on RNA or protein function, based on experimental evidence from submitters.
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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.
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Allele frequency
Help
The frequency of the allele represented by this VCV record.
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- 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 |
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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Uncertain significance (1) |
criteria provided, single submitter
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Mar 12, 2023 | RCV001983479.7 | |
Conflicting interpretations of pathogenicity (2) |
criteria provided, conflicting classifications
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Mar 23, 2023 | RCV002398066.6 |
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
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Hereditary cancer-predisposing syndrome
Affected status: unknown
Allele origin:
germline
|
University of Washington Department of Laboratory Medicine, University of Washington
Accession: SCV003851133.1
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
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Comment:
Missense variant in a coldspot region where missense variants are very unlikely to be pathogenic (PMID:31911673).
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Uncertain significance
(Mar 12, 2023)
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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: SCV002268023.3
First in ClinVar: Mar 28, 2022 Last updated: Feb 28, 2024 |
Comment:
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 … (more)
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. ClinVar contains an entry for this variant (Variation ID: 1489883). This variant has not been reported in the literature in individuals affected with BRCA1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces asparagine, which is neutral and polar, with serine, which is neutral and polar, at codon 555 of the BRCA1 protein (p.Asn555Ser). (less)
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Uncertain significance
(Sep 23, 2020)
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criteria provided, single submitter
Method: clinical testing
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Hereditary cancer-predisposing syndrome
Affected status: unknown
Allele origin:
germline
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Ambry Genetics
Accession: SCV002706573.2
First in ClinVar: Nov 29, 2022 Last updated: May 01, 2024 |
Comment:
The p.N555S variant (also known as c.1664A>G), located in coding exon 9 of the BRCA1 gene, results from an A to G substitution at nucleotide … (more)
The p.N555S variant (also known as c.1664A>G), located in coding exon 9 of the BRCA1 gene, results from an A to G substitution at nucleotide position 1664. The asparagine at codon 555 is replaced by serine, an amino acid with highly 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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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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- | - | - | - | PMID: 31911673 |
Text-mined citations for rs2154431398 ...
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.