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. Experimental studies have shown that this missense change affects BRCA1 function (PMID: 30209399). Advanced modeling performed at Invitae incorporating data from internal and/or published experimental studies (PMID: 30209399) indicates that this missense variant is expected to disrupt BRCA1 function. ClinVar contains an entry for this variant (Variation ID: 96943). 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 glutamic acid, which is acidic and polar, with aspartic acid, which is acidic and polar, at codon 1735 of the BRCA1 protein (p.Glu1735Asp).
ClinVar Genomic variation as it relates to human health
NM_007294.4(BRCA1):c.5205A>T (p.Glu1735Asp)
Germline
Classification
Help
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.
(3)
Help
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
3
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Variant Details
- Identifiers
-
NM_007294.4(BRCA1):c.5205A>T (p.Glu1735Asp)
Variation ID: 96943 Accession: VCV000096943.10
- Type and length
-
single nucleotide variant, 1 bp
- Location
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Cytogenetic: 17q21.31 17: 43057124 (GRCh38) [ NCBI UCSC ] 17: 41209141 (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 Sep 27, 2014 Feb 28, 2024 Sep 10, 2023 - HGVS
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... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_007294.4:c.5205A>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_009225.1:p.Glu1735Asp missense NM_001407571.1:c.4992A>T NP_001394500.1:p.Glu1664Asp missense NM_001407581.1:c.5271A>T NP_001394510.1:p.Glu1757Asp missense NM_001407582.1:c.5271A>T NP_001394511.1:p.Glu1757Asp missense NM_001407583.1:c.5268A>T NP_001394512.1:p.Glu1756Asp missense NM_001407585.1:c.5268A>T NP_001394514.1:p.Glu1756Asp missense NM_001407587.1:c.5268A>T NP_001394516.1:p.Glu1756Asp missense NM_001407590.1:c.5265A>T NP_001394519.1:p.Glu1755Asp missense NM_001407591.1:c.5265A>T NP_001394520.1:p.Glu1755Asp missense NM_001407593.1:c.5205A>T NP_001394522.1:p.Glu1735Asp missense NM_001407594.1:c.5205A>T NP_001394523.1:p.Glu1735Asp missense NM_001407596.1:c.5205A>T NP_001394525.1:p.Glu1735Asp missense NM_001407597.1:c.5205A>T NP_001394526.1:p.Glu1735Asp missense NM_001407598.1:c.5205A>T NP_001394527.1:p.Glu1735Asp missense NM_001407602.1:c.5205A>T NP_001394531.1:p.Glu1735Asp missense NM_001407603.1:c.5205A>T NP_001394532.1:p.Glu1735Asp missense NM_001407605.1:c.5205A>T NP_001394534.1:p.Glu1735Asp missense NM_001407610.1:c.5202A>T NP_001394539.1:p.Glu1734Asp missense NM_001407611.1:c.5202A>T NP_001394540.1:p.Glu1734Asp missense NM_001407612.1:c.5202A>T NP_001394541.1:p.Glu1734Asp missense NM_001407613.1:c.5202A>T NP_001394542.1:p.Glu1734Asp missense NM_001407614.1:c.5202A>T NP_001394543.1:p.Glu1734Asp missense NM_001407615.1:c.5202A>T NP_001394544.1:p.Glu1734Asp missense NM_001407616.1:c.5202A>T NP_001394545.1:p.Glu1734Asp missense NM_001407617.1:c.5202A>T NP_001394546.1:p.Glu1734Asp missense NM_001407618.1:c.5202A>T NP_001394547.1:p.Glu1734Asp missense NM_001407619.1:c.5202A>T NP_001394548.1:p.Glu1734Asp missense NM_001407620.1:c.5202A>T NP_001394549.1:p.Glu1734Asp missense NM_001407621.1:c.5202A>T NP_001394550.1:p.Glu1734Asp missense NM_001407622.1:c.5202A>T NP_001394551.1:p.Glu1734Asp missense NM_001407623.1:c.5202A>T NP_001394552.1:p.Glu1734Asp missense NM_001407624.1:c.5202A>T NP_001394553.1:p.Glu1734Asp missense NM_001407625.1:c.5202A>T NP_001394554.1:p.Glu1734Asp missense NM_001407626.1:c.5202A>T NP_001394555.1:p.Glu1734Asp missense NM_001407627.1:c.5199A>T NP_001394556.1:p.Glu1733Asp missense NM_001407628.1:c.5199A>T NP_001394557.1:p.Glu1733Asp missense NM_001407629.1:c.5199A>T NP_001394558.1:p.Glu1733Asp missense NM_001407630.1:c.5199A>T NP_001394559.1:p.Glu1733Asp missense NM_001407631.1:c.5199A>T NP_001394560.1:p.Glu1733Asp missense NM_001407632.1:c.5199A>T NP_001394561.1:p.Glu1733Asp missense NM_001407633.1:c.5199A>T NP_001394562.1:p.Glu1733Asp missense NM_001407634.1:c.5199A>T NP_001394563.1:p.Glu1733Asp missense NM_001407635.1:c.5199A>T NP_001394564.1:p.Glu1733Asp missense NM_001407636.1:c.5199A>T NP_001394565.1:p.Glu1733Asp missense NM_001407637.1:c.5199A>T NP_001394566.1:p.Glu1733Asp missense NM_001407638.1:c.5199A>T NP_001394567.1:p.Glu1733Asp missense NM_001407639.1:c.5199A>T NP_001394568.1:p.Glu1733Asp missense NM_001407640.1:c.5199A>T NP_001394569.1:p.Glu1733Asp missense NM_001407641.1:c.5199A>T NP_001394570.1:p.Glu1733Asp missense NM_001407642.1:c.5199A>T NP_001394571.1:p.Glu1733Asp missense NM_001407644.1:c.5196A>T NP_001394573.1:p.Glu1732Asp missense NM_001407645.1:c.5196A>T NP_001394574.1:p.Glu1732Asp missense NM_001407646.1:c.5193A>T NP_001394575.1:p.Glu1731Asp missense NM_001407647.1:c.5190A>T NP_001394576.1:p.Glu1730Asp missense NM_001407648.1:c.5148A>T NP_001394577.1:p.Glu1716Asp missense NM_001407649.1:c.5145A>T NP_001394578.1:p.Glu1715Asp missense NM_001407652.1:c.5127A>T NP_001394581.1:p.Glu1709Asp missense NM_001407653.1:c.5127A>T NP_001394582.1:p.Glu1709Asp missense NM_001407654.1:c.5127A>T NP_001394583.1:p.Glu1709Asp missense NM_001407655.1:c.5127A>T NP_001394584.1:p.Glu1709Asp missense NM_001407656.1:c.5124A>T NP_001394585.1:p.Glu1708Asp missense NM_001407657.1:c.5124A>T NP_001394586.1:p.Glu1708Asp missense NM_001407658.1:c.5124A>T NP_001394587.1:p.Glu1708Asp missense NM_001407659.1:c.5121A>T NP_001394588.1:p.Glu1707Asp missense NM_001407660.1:c.5121A>T NP_001394589.1:p.Glu1707Asp missense NM_001407661.1:c.5121A>T NP_001394590.1:p.Glu1707Asp missense NM_001407662.1:c.5121A>T NP_001394591.1:p.Glu1707Asp missense NM_001407663.1:c.5121A>T NP_001394592.1:p.Glu1707Asp missense NM_001407664.1:c.5082A>T NP_001394593.1:p.Glu1694Asp missense NM_001407665.1:c.5082A>T NP_001394594.1:p.Glu1694Asp missense NM_001407666.1:c.5082A>T NP_001394595.1:p.Glu1694Asp missense NM_001407667.1:c.5082A>T NP_001394596.1:p.Glu1694Asp missense NM_001407668.1:c.5082A>T NP_001394597.1:p.Glu1694Asp missense NM_001407669.1:c.5082A>T NP_001394598.1:p.Glu1694Asp missense NM_001407670.1:c.5079A>T NP_001394599.1:p.Glu1693Asp missense NM_001407671.1:c.5079A>T NP_001394600.1:p.Glu1693Asp missense NM_001407672.1:c.5079A>T NP_001394601.1:p.Glu1693Asp missense NM_001407673.1:c.5079A>T NP_001394602.1:p.Glu1693Asp missense NM_001407674.1:c.5079A>T NP_001394603.1:p.Glu1693Asp missense NM_001407675.1:c.5079A>T NP_001394604.1:p.Glu1693Asp missense NM_001407676.1:c.5079A>T NP_001394605.1:p.Glu1693Asp missense NM_001407677.1:c.5079A>T NP_001394606.1:p.Glu1693Asp missense NM_001407678.1:c.5079A>T NP_001394607.1:p.Glu1693Asp missense NM_001407679.1:c.5079A>T NP_001394608.1:p.Glu1693Asp missense NM_001407680.1:c.5079A>T NP_001394609.1:p.Glu1693Asp missense NM_001407681.1:c.5076A>T NP_001394610.1:p.Glu1692Asp missense NM_001407682.1:c.5076A>T NP_001394611.1:p.Glu1692Asp missense NM_001407683.1:c.5076A>T NP_001394612.1:p.Glu1692Asp missense NM_001407684.1:c.5205A>T NP_001394613.1:p.Glu1735Asp missense NM_001407685.1:c.5076A>T NP_001394614.1:p.Glu1692Asp missense NM_001407686.1:c.5076A>T NP_001394615.1:p.Glu1692Asp missense NM_001407687.1:c.5076A>T NP_001394616.1:p.Glu1692Asp missense NM_001407688.1:c.5076A>T NP_001394617.1:p.Glu1692Asp missense NM_001407689.1:c.5076A>T NP_001394618.1:p.Glu1692Asp missense NM_001407690.1:c.5073A>T NP_001394619.1:p.Glu1691Asp missense NM_001407691.1:c.5073A>T NP_001394620.1:p.Glu1691Asp missense NM_001407692.1:c.5064A>T NP_001394621.1:p.Glu1688Asp missense NM_001407694.1:c.5064A>T NP_001394623.1:p.Glu1688Asp missense NM_001407695.1:c.5064A>T NP_001394624.1:p.Glu1688Asp missense NM_001407696.1:c.5064A>T NP_001394625.1:p.Glu1688Asp missense NM_001407697.1:c.5064A>T NP_001394626.1:p.Glu1688Asp missense NM_001407698.1:c.5064A>T NP_001394627.1:p.Glu1688Asp missense NM_001407724.1:c.5064A>T NP_001394653.1:p.Glu1688Asp missense NM_001407725.1:c.5064A>T NP_001394654.1:p.Glu1688Asp missense NM_001407726.1:c.5064A>T NP_001394655.1:p.Glu1688Asp missense NM_001407727.1:c.5064A>T NP_001394656.1:p.Glu1688Asp missense NM_001407728.1:c.5064A>T NP_001394657.1:p.Glu1688Asp missense NM_001407729.1:c.5064A>T NP_001394658.1:p.Glu1688Asp missense NM_001407730.1:c.5064A>T NP_001394659.1:p.Glu1688Asp missense NM_001407731.1:c.5064A>T NP_001394660.1:p.Glu1688Asp missense NM_001407732.1:c.5061A>T NP_001394661.1:p.Glu1687Asp missense NM_001407733.1:c.5061A>T NP_001394662.1:p.Glu1687Asp missense NM_001407734.1:c.5061A>T NP_001394663.1:p.Glu1687Asp missense NM_001407735.1:c.5061A>T NP_001394664.1:p.Glu1687Asp missense NM_001407736.1:c.5061A>T NP_001394665.1:p.Glu1687Asp missense NM_001407737.1:c.5061A>T NP_001394666.1:p.Glu1687Asp missense NM_001407738.1:c.5061A>T NP_001394667.1:p.Glu1687Asp missense NM_001407739.1:c.5061A>T NP_001394668.1:p.Glu1687Asp missense NM_001407740.1:c.5061A>T NP_001394669.1:p.Glu1687Asp missense NM_001407741.1:c.5061A>T NP_001394670.1:p.Glu1687Asp missense NM_001407742.1:c.5061A>T NP_001394671.1:p.Glu1687Asp missense NM_001407743.1:c.5061A>T NP_001394672.1:p.Glu1687Asp missense NM_001407744.1:c.5061A>T NP_001394673.1:p.Glu1687Asp missense NM_001407745.1:c.5061A>T NP_001394674.1:p.Glu1687Asp missense NM_001407746.1:c.5061A>T NP_001394675.1:p.Glu1687Asp missense NM_001407747.1:c.5061A>T NP_001394676.1:p.Glu1687Asp missense NM_001407748.1:c.5061A>T NP_001394677.1:p.Glu1687Asp missense NM_001407749.1:c.5061A>T NP_001394678.1:p.Glu1687Asp missense NM_001407750.1:c.5061A>T NP_001394679.1:p.Glu1687Asp missense NM_001407751.1:c.5061A>T NP_001394680.1:p.Glu1687Asp missense NM_001407752.1:c.5061A>T NP_001394681.1:p.Glu1687Asp missense NM_001407838.1:c.5058A>T NP_001394767.1:p.Glu1686Asp missense NM_001407839.1:c.5058A>T NP_001394768.1:p.Glu1686Asp missense NM_001407841.1:c.5058A>T NP_001394770.1:p.Glu1686Asp missense NM_001407842.1:c.5058A>T NP_001394771.1:p.Glu1686Asp missense NM_001407843.1:c.5058A>T NP_001394772.1:p.Glu1686Asp missense NM_001407844.1:c.5058A>T NP_001394773.1:p.Glu1686Asp missense NM_001407845.1:c.5058A>T NP_001394774.1:p.Glu1686Asp missense NM_001407846.1:c.5058A>T NP_001394775.1:p.Glu1686Asp missense NM_001407847.1:c.5058A>T NP_001394776.1:p.Glu1686Asp missense NM_001407848.1:c.5058A>T NP_001394777.1:p.Glu1686Asp missense NM_001407849.1:c.5058A>T NP_001394778.1:p.Glu1686Asp missense NM_001407850.1:c.5058A>T NP_001394779.1:p.Glu1686Asp missense NM_001407851.1:c.5058A>T NP_001394780.1:p.Glu1686Asp missense NM_001407852.1:c.5058A>T NP_001394781.1:p.Glu1686Asp missense NM_001407853.1:c.5058A>T NP_001394782.1:p.Glu1686Asp missense NM_001407854.1:c.5205A>T NP_001394783.1:p.Glu1735Asp missense NM_001407858.1:c.5202A>T NP_001394787.1:p.Glu1734Asp missense NM_001407859.1:c.5202A>T NP_001394788.1:p.Glu1734Asp missense NM_001407860.1:c.5202A>T NP_001394789.1:p.Glu1734Asp missense NM_001407861.1:c.5199A>T NP_001394790.1:p.Glu1733Asp missense NM_001407862.1:c.5004A>T NP_001394791.1:p.Glu1668Asp missense NM_001407863.1:c.5001A>T NP_001394792.1:p.Glu1667Asp missense NM_001407874.1:c.4998A>T NP_001394803.1:p.Glu1666Asp missense NM_001407875.1:c.4998A>T NP_001394804.1:p.Glu1666Asp missense NM_001407879.1:c.4995A>T NP_001394808.1:p.Glu1665Asp missense NM_001407881.1:c.4995A>T NP_001394810.1:p.Glu1665Asp missense NM_001407882.1:c.4995A>T NP_001394811.1:p.Glu1665Asp missense NM_001407884.1:c.4995A>T NP_001394813.1:p.Glu1665Asp missense NM_001407885.1:c.4995A>T NP_001394814.1:p.Glu1665Asp missense NM_001407886.1:c.4995A>T NP_001394815.1:p.Glu1665Asp missense NM_001407887.1:c.4995A>T NP_001394816.1:p.Glu1665Asp missense NM_001407889.1:c.4995A>T NP_001394818.1:p.Glu1665Asp missense NM_001407894.1:c.4992A>T NP_001394823.1:p.Glu1664Asp missense NM_001407895.1:c.4992A>T NP_001394824.1:p.Glu1664Asp missense NM_001407896.1:c.4992A>T NP_001394825.1:p.Glu1664Asp missense NM_001407897.1:c.4992A>T NP_001394826.1:p.Glu1664Asp missense NM_001407898.1:c.4992A>T NP_001394827.1:p.Glu1664Asp missense NM_001407899.1:c.4992A>T NP_001394828.1:p.Glu1664Asp missense NM_001407900.1:c.4992A>T NP_001394829.1:p.Glu1664Asp missense NM_001407902.1:c.4992A>T NP_001394831.1:p.Glu1664Asp missense NM_001407904.1:c.4992A>T NP_001394833.1:p.Glu1664Asp missense NM_001407906.1:c.4992A>T NP_001394835.1:p.Glu1664Asp missense NM_001407907.1:c.4992A>T NP_001394836.1:p.Glu1664Asp missense NM_001407908.1:c.4992A>T NP_001394837.1:p.Glu1664Asp missense NM_001407909.1:c.4992A>T NP_001394838.1:p.Glu1664Asp missense NM_001407910.1:c.4992A>T NP_001394839.1:p.Glu1664Asp missense NM_001407915.1:c.4989A>T NP_001394844.1:p.Glu1663Asp missense NM_001407916.1:c.4989A>T NP_001394845.1:p.Glu1663Asp missense NM_001407917.1:c.4989A>T NP_001394846.1:p.Glu1663Asp missense NM_001407918.1:c.4989A>T NP_001394847.1:p.Glu1663Asp missense NM_001407919.1:c.5082A>T NP_001394848.1:p.Glu1694Asp missense NM_001407920.1:c.4941A>T NP_001394849.1:p.Glu1647Asp missense NM_001407921.1:c.4941A>T NP_001394850.1:p.Glu1647Asp missense NM_001407922.1:c.4941A>T NP_001394851.1:p.Glu1647Asp missense NM_001407923.1:c.4941A>T NP_001394852.1:p.Glu1647Asp missense NM_001407924.1:c.4941A>T NP_001394853.1:p.Glu1647Asp missense NM_001407925.1:c.4941A>T NP_001394854.1:p.Glu1647Asp missense NM_001407926.1:c.4941A>T NP_001394855.1:p.Glu1647Asp missense NM_001407927.1:c.4938A>T NP_001394856.1:p.Glu1646Asp missense NM_001407928.1:c.4938A>T NP_001394857.1:p.Glu1646Asp missense NM_001407929.1:c.4938A>T NP_001394858.1:p.Glu1646Asp missense NM_001407930.1:c.4938A>T NP_001394859.1:p.Glu1646Asp missense NM_001407931.1:c.4938A>T NP_001394860.1:p.Glu1646Asp missense NM_001407932.1:c.4938A>T NP_001394861.1:p.Glu1646Asp missense NM_001407933.1:c.4938A>T NP_001394862.1:p.Glu1646Asp missense NM_001407934.1:c.4935A>T NP_001394863.1:p.Glu1645Asp missense NM_001407935.1:c.4935A>T NP_001394864.1:p.Glu1645Asp missense NM_001407936.1:c.4935A>T NP_001394865.1:p.Glu1645Asp missense NM_001407937.1:c.5082A>T NP_001394866.1:p.Glu1694Asp missense NM_001407938.1:c.5082A>T NP_001394867.1:p.Glu1694Asp missense NM_001407939.1:c.5079A>T NP_001394868.1:p.Glu1693Asp missense NM_001407940.1:c.5079A>T NP_001394869.1:p.Glu1693Asp missense NM_001407941.1:c.5076A>T NP_001394870.1:p.Glu1692Asp missense NM_001407942.1:c.5064A>T NP_001394871.1:p.Glu1688Asp missense NM_001407943.1:c.5061A>T NP_001394872.1:p.Glu1687Asp missense NM_001407944.1:c.5061A>T NP_001394873.1:p.Glu1687Asp missense NM_001407945.1:c.5061A>T NP_001394874.1:p.Glu1687Asp missense NM_001407946.1:c.4872A>T NP_001394875.1:p.Glu1624Asp missense NM_001407947.1:c.4872A>T NP_001394876.1:p.Glu1624Asp missense NM_001407948.1:c.4872A>T NP_001394877.1:p.Glu1624Asp missense NM_001407949.1:c.4872A>T NP_001394878.1:p.Glu1624Asp missense NM_001407950.1:c.4869A>T NP_001394879.1:p.Glu1623Asp missense NM_001407951.1:c.4869A>T NP_001394880.1:p.Glu1623Asp missense NM_001407952.1:c.4869A>T NP_001394881.1:p.Glu1623Asp missense NM_001407953.1:c.4869A>T NP_001394882.1:p.Glu1623Asp missense NM_001407954.1:c.4869A>T NP_001394883.1:p.Glu1623Asp missense NM_001407955.1:c.4869A>T NP_001394884.1:p.Glu1623Asp missense NM_001407956.1:c.4866A>T NP_001394885.1:p.Glu1622Asp missense NM_001407957.1:c.4866A>T NP_001394886.1:p.Glu1622Asp missense NM_001407958.1:c.4866A>T NP_001394887.1:p.Glu1622Asp missense NM_001407959.1:c.4824A>T NP_001394888.1:p.Glu1608Asp missense NM_001407960.1:c.4821A>T NP_001394889.1:p.Glu1607Asp missense NM_001407962.1:c.4821A>T NP_001394891.1:p.Glu1607Asp missense NM_001407963.1:c.4818A>T NP_001394892.1:p.Glu1606Asp missense NM_001407964.1:c.4743A>T NP_001394893.1:p.Glu1581Asp missense NM_001407965.1:c.4698A>T NP_001394894.1:p.Glu1566Asp missense NM_001407966.1:c.4317A>T NP_001394895.1:p.Glu1439Asp missense NM_001407967.1:c.4314A>T NP_001394896.1:p.Glu1438Asp missense NM_001407968.1:c.2601A>T NP_001394897.1:p.Glu867Asp missense NM_001407969.1:c.2598A>T NP_001394898.1:p.Glu866Asp missense NM_001407970.1:c.1962A>T NP_001394899.1:p.Glu654Asp missense NM_001407971.1:c.1962A>T NP_001394900.1:p.Glu654Asp missense NM_001407972.1:c.1959A>T NP_001394901.1:p.Glu653Asp missense NM_001407973.1:c.1896A>T NP_001394902.1:p.Glu632Asp missense NM_001407974.1:c.1896A>T NP_001394903.1:p.Glu632Asp missense NM_001407975.1:c.1896A>T NP_001394904.1:p.Glu632Asp missense NM_001407976.1:c.1896A>T NP_001394905.1:p.Glu632Asp missense NM_001407977.1:c.1896A>T NP_001394906.1:p.Glu632Asp missense NM_001407978.1:c.1896A>T NP_001394907.1:p.Glu632Asp missense NM_001407979.1:c.1893A>T NP_001394908.1:p.Glu631Asp missense NM_001407980.1:c.1893A>T NP_001394909.1:p.Glu631Asp missense NM_001407981.1:c.1893A>T NP_001394910.1:p.Glu631Asp missense NM_001407982.1:c.1893A>T NP_001394911.1:p.Glu631Asp missense NM_001407983.1:c.1893A>T NP_001394912.1:p.Glu631Asp missense NM_001407984.1:c.1893A>T NP_001394913.1:p.Glu631Asp missense NM_001407985.1:c.1893A>T NP_001394914.1:p.Glu631Asp missense NM_001407986.1:c.1893A>T NP_001394915.1:p.Glu631Asp missense NM_001407990.1:c.1893A>T NP_001394919.1:p.Glu631Asp missense NM_001407991.1:c.1893A>T NP_001394920.1:p.Glu631Asp missense NM_001407992.1:c.1893A>T NP_001394921.1:p.Glu631Asp missense NM_001407993.1:c.1893A>T NP_001394922.1:p.Glu631Asp missense NM_001408392.1:c.1890A>T NP_001395321.1:p.Glu630Asp missense NM_001408396.1:c.1890A>T NP_001395325.1:p.Glu630Asp missense NM_001408397.1:c.1890A>T NP_001395326.1:p.Glu630Asp missense NM_001408398.1:c.1890A>T NP_001395327.1:p.Glu630Asp missense NM_001408399.1:c.1890A>T NP_001395328.1:p.Glu630Asp missense NM_001408400.1:c.1890A>T NP_001395329.1:p.Glu630Asp missense NM_001408401.1:c.1890A>T NP_001395330.1:p.Glu630Asp missense NM_001408402.1:c.1890A>T NP_001395331.1:p.Glu630Asp missense NM_001408403.1:c.1890A>T NP_001395332.1:p.Glu630Asp missense NM_001408404.1:c.1890A>T NP_001395333.1:p.Glu630Asp missense NM_001408406.1:c.1887A>T NP_001395335.1:p.Glu629Asp missense NM_001408407.1:c.1887A>T NP_001395336.1:p.Glu629Asp missense NM_001408408.1:c.1887A>T NP_001395337.1:p.Glu629Asp missense NM_001408409.1:c.1884A>T NP_001395338.1:p.Glu628Asp missense NM_001408410.1:c.1821A>T NP_001395339.1:p.Glu607Asp missense NM_001408411.1:c.1818A>T NP_001395340.1:p.Glu606Asp missense NM_001408412.1:c.1815A>T NP_001395341.1:p.Glu605Asp missense NM_001408413.1:c.1815A>T NP_001395342.1:p.Glu605Asp missense NM_001408414.1:c.1815A>T NP_001395343.1:p.Glu605Asp missense NM_001408415.1:c.1815A>T NP_001395344.1:p.Glu605Asp missense NM_001408416.1:c.1815A>T NP_001395345.1:p.Glu605Asp missense NM_001408418.1:c.1779A>T NP_001395347.1:p.Glu593Asp missense NM_001408419.1:c.1779A>T NP_001395348.1:p.Glu593Asp missense NM_001408420.1:c.1779A>T NP_001395349.1:p.Glu593Asp missense NM_001408421.1:c.1776A>T NP_001395350.1:p.Glu592Asp missense NM_001408422.1:c.1776A>T NP_001395351.1:p.Glu592Asp missense NM_001408423.1:c.1776A>T NP_001395352.1:p.Glu592Asp missense NM_001408424.1:c.1776A>T NP_001395353.1:p.Glu592Asp missense NM_001408425.1:c.1773A>T NP_001395354.1:p.Glu591Asp missense NM_001408426.1:c.1773A>T NP_001395355.1:p.Glu591Asp missense NM_001408427.1:c.1773A>T NP_001395356.1:p.Glu591Asp missense NM_001408428.1:c.1773A>T NP_001395357.1:p.Glu591Asp missense NM_001408429.1:c.1773A>T NP_001395358.1:p.Glu591Asp missense NM_001408430.1:c.1773A>T NP_001395359.1:p.Glu591Asp missense NM_001408431.1:c.1773A>T NP_001395360.1:p.Glu591Asp missense NM_001408432.1:c.1770A>T NP_001395361.1:p.Glu590Asp missense NM_001408433.1:c.1770A>T NP_001395362.1:p.Glu590Asp missense NM_001408434.1:c.1770A>T NP_001395363.1:p.Glu590Asp missense NM_001408435.1:c.1770A>T NP_001395364.1:p.Glu590Asp missense NM_001408436.1:c.1770A>T NP_001395365.1:p.Glu590Asp missense NM_001408437.1:c.1770A>T NP_001395366.1:p.Glu590Asp missense NM_001408438.1:c.1770A>T NP_001395367.1:p.Glu590Asp missense NM_001408439.1:c.1770A>T NP_001395368.1:p.Glu590Asp missense NM_001408440.1:c.1770A>T NP_001395369.1:p.Glu590Asp missense NM_001408441.1:c.1770A>T NP_001395370.1:p.Glu590Asp missense NM_001408442.1:c.1770A>T NP_001395371.1:p.Glu590Asp missense NM_001408443.1:c.1770A>T NP_001395372.1:p.Glu590Asp missense NM_001408444.1:c.1770A>T NP_001395373.1:p.Glu590Asp missense NM_001408445.1:c.1767A>T NP_001395374.1:p.Glu589Asp missense NM_001408446.1:c.1767A>T NP_001395375.1:p.Glu589Asp missense NM_001408447.1:c.1767A>T NP_001395376.1:p.Glu589Asp missense NM_001408448.1:c.1767A>T NP_001395377.1:p.Glu589Asp missense NM_001408450.1:c.1767A>T NP_001395379.1:p.Glu589Asp missense NM_001408451.1:c.1761A>T NP_001395380.1:p.Glu587Asp missense NM_001408452.1:c.1755A>T NP_001395381.1:p.Glu585Asp missense NM_001408453.1:c.1755A>T NP_001395382.1:p.Glu585Asp missense NM_001408454.1:c.1755A>T NP_001395383.1:p.Glu585Asp missense NM_001408455.1:c.1755A>T NP_001395384.1:p.Glu585Asp missense NM_001408456.1:c.1755A>T NP_001395385.1:p.Glu585Asp missense NM_001408457.1:c.1755A>T NP_001395386.1:p.Glu585Asp missense NM_001408458.1:c.1752A>T NP_001395387.1:p.Glu584Asp missense NM_001408459.1:c.1752A>T NP_001395388.1:p.Glu584Asp missense NM_001408460.1:c.1752A>T NP_001395389.1:p.Glu584Asp missense NM_001408461.1:c.1752A>T NP_001395390.1:p.Glu584Asp missense NM_001408462.1:c.1752A>T NP_001395391.1:p.Glu584Asp missense NM_001408463.1:c.1752A>T NP_001395392.1:p.Glu584Asp missense NM_001408464.1:c.1752A>T NP_001395393.1:p.Glu584Asp missense NM_001408465.1:c.1752A>T NP_001395394.1:p.Glu584Asp missense NM_001408466.1:c.1752A>T NP_001395395.1:p.Glu584Asp missense NM_001408467.1:c.1752A>T NP_001395396.1:p.Glu584Asp missense NM_001408468.1:c.1749A>T NP_001395397.1:p.Glu583Asp missense NM_001408469.1:c.1749A>T NP_001395398.1:p.Glu583Asp missense NM_001408470.1:c.1749A>T NP_001395399.1:p.Glu583Asp missense NM_001408472.1:c.1893A>T NP_001395401.1:p.Glu631Asp missense NM_001408473.1:c.1890A>T NP_001395402.1:p.Glu630Asp missense NM_001408474.1:c.1695A>T NP_001395403.1:p.Glu565Asp missense NM_001408475.1:c.1692A>T NP_001395404.1:p.Glu564Asp missense NM_001408476.1:c.1692A>T NP_001395405.1:p.Glu564Asp missense NM_001408478.1:c.1686A>T NP_001395407.1:p.Glu562Asp missense NM_001408479.1:c.1686A>T NP_001395408.1:p.Glu562Asp missense NM_001408480.1:c.1686A>T NP_001395409.1:p.Glu562Asp missense NM_001408481.1:c.1683A>T NP_001395410.1:p.Glu561Asp missense NM_001408482.1:c.1683A>T NP_001395411.1:p.Glu561Asp missense NM_001408483.1:c.1683A>T NP_001395412.1:p.Glu561Asp missense NM_001408484.1:c.1683A>T NP_001395413.1:p.Glu561Asp missense NM_001408485.1:c.1683A>T NP_001395414.1:p.Glu561Asp missense NM_001408489.1:c.1683A>T NP_001395418.1:p.Glu561Asp missense NM_001408490.1:c.1683A>T NP_001395419.1:p.Glu561Asp missense NM_001408491.1:c.1683A>T NP_001395420.1:p.Glu561Asp missense NM_001408492.1:c.1680A>T NP_001395421.1:p.Glu560Asp missense NM_001408493.1:c.1680A>T NP_001395422.1:p.Glu560Asp missense NM_001408494.1:c.1656A>T NP_001395423.1:p.Glu552Asp missense NM_001408495.1:c.1650A>T NP_001395424.1:p.Glu550Asp missense NM_001408496.1:c.1632A>T NP_001395425.1:p.Glu544Asp missense NM_001408497.1:c.1632A>T NP_001395426.1:p.Glu544Asp missense NM_001408498.1:c.1632A>T NP_001395427.1:p.Glu544Asp missense NM_001408499.1:c.1632A>T NP_001395428.1:p.Glu544Asp missense NM_001408500.1:c.1632A>T NP_001395429.1:p.Glu544Asp missense NM_001408501.1:c.1632A>T NP_001395430.1:p.Glu544Asp missense NM_001408502.1:c.1629A>T NP_001395431.1:p.Glu543Asp missense NM_001408503.1:c.1629A>T NP_001395432.1:p.Glu543Asp missense NM_001408504.1:c.1629A>T NP_001395433.1:p.Glu543Asp missense NM_001408505.1:c.1626A>T NP_001395434.1:p.Glu542Asp missense NM_001408506.1:c.1569A>T NP_001395435.1:p.Glu523Asp missense NM_001408507.1:c.1566A>T NP_001395436.1:p.Glu522Asp missense NM_001408508.1:c.1557A>T NP_001395437.1:p.Glu519Asp missense NM_001408509.1:c.1554A>T NP_001395438.1:p.Glu518Asp missense NM_001408510.1:c.1515A>T NP_001395439.1:p.Glu505Asp missense NM_001408511.1:c.1512A>T NP_001395440.1:p.Glu504Asp missense NM_001408512.1:c.1392A>T NP_001395441.1:p.Glu464Asp missense NM_001408513.1:c.1365A>T NP_001395442.1:p.Glu455Asp missense NM_001408514.1:c.969A>T NP_001395443.1:p.Glu323Asp missense NM_007297.4:c.5064A>T NP_009228.2:p.Glu1688Asp missense NM_007298.4:c.1893A>T NP_009229.2:p.Glu631Asp missense NM_007299.4:c.1893A>T NP_009230.2:p.Glu631Asp missense NM_007300.4:c.5268A>T NP_009231.2:p.Glu1756Asp missense NM_007304.2:c.1893A>T NP_009235.2:p.Glu631Asp missense NR_027676.2:n.5382A>T non-coding transcript variant NC_000017.11:g.43057124T>A NC_000017.10:g.41209141T>A NG_005905.2:g.160860A>T LRG_292:g.160860A>T LRG_292t1:c.5205A>T LRG_292p1:p.Glu1735Asp - Protein change
- E1735D, E1688D, E1756D, E631D, E1438D, E1608D, E1665D, E1666D, E1691D, E1693D, E1716D, E1734D, E1755D, E323D, E464D, E522D, E523D, E543D, E583D, E584D, E589D, E605D, E606D, E607D, E628D, E629D, E1581D, E1607D, E1622D, E1663D, E1686D, E1692D, E1708D, E1715D, E1731D, E1733D, E518D, E560D, E587D, E591D, E630D, E653D, E867D, E1439D, E1566D, E1624D, E1645D, E1647D, E1707D, E1732D, E455D, E504D, E542D, E544D, E550D, E562D, E565D, E585D, E590D, E1606D, E1623D, E1646D, E1664D, E1667D, E1668D, E1687D, E1694D, E1709D, E1730D, E1757D, E505D, E519D, E552D, E561D, E564D, E592D, E593D, E632D, E654D, E866D
- Other names
-
5324A>T
- Canonical SPDI
- NC_000017.11:43057123:T:A
-
Functional
consequence HelpThe effect of the variant on RNA or protein function, based on experimental evidence from submitters.
-
functionally_abnormal; Sequence Ontology [ SO:0002218]The saturation genome editing (SGE) assay for BRCA1 NM_007294.3:c.5205A>T, a MISSENSE variant, produced a function score of -1.37, corresponding to a functional classification of LOSS_OF_FUNCTION. SGE function score ranges for classification are as follows: ‘functional’, score > -0.748; ‘intermediate’, -0.748 > score > -1.328; ‘non-functional’, score < -1.328. The median synonymous SNV scored 0.0 and the median nonsense SNV scored -2.12. [submitted by Brotman Baty Institute, University of Washington]
-
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.
- -
- 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 | ||
|---|---|---|---|---|---|---|
| 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. |
|||
| BRCA1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
13044 | 14850 | |
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. |
|---|---|---|---|---|
| Uncertain significance (2) |
no assertion criteria provided
|
Mar 19, 2008 | RCV000083064.6 | |
| Uncertain significance (1) |
criteria provided, single submitter
|
Sep 10, 2023 | RCV000205011.8 |
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. |
|
|---|---|---|---|---|---|
|
Uncertain significance
(Sep 10, 2023)
|
criteria provided, single submitter
Method: clinical testing
|
Hereditary breast ovarian cancer syndrome
Affected status: unknown
Allele origin:
germline
|
Labcorp Genetics (formerly Invitae), Labcorp
Accession: SCV000260014.5
First in ClinVar: Jan 31, 2016 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. Experimental studies have shown that this missense change affects BRCA1 function (PMID: 30209399). Advanced modeling performed at Invitae incorporating data from internal and/or published experimental studies (PMID: 30209399) indicates that this missense variant is expected to disrupt BRCA1 function. ClinVar contains an entry for this variant (Variation ID: 96943). 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 glutamic acid, which is acidic and polar, with aspartic acid, which is acidic and polar, at codon 1735 of the BRCA1 protein (p.Glu1735Asp). (less)
|
|
|
Uncertain significance
(Mar 19, 2008)
|
no assertion criteria provided
Method: clinical testing
|
Breast-ovarian cancer, familial 1
Affected status: not provided
Allele origin:
germline
|
Sharing Clinical Reports Project (SCRP)
Accession: SCV000115138.4
First in ClinVar: Feb 09, 2014 Last updated: Sep 27, 2014 |
|
|
|
not provided
(-)
|
no classification provided
Method: in vitro
|
Breast-ovarian cancer, familial 1
Affected status: not applicable
Allele origin:
not applicable
|
Brotman Baty Institute, University of Washington
Accession: SCV001241926.1
First in ClinVar: Apr 18, 2020 Last updated: Apr 18, 2020 |
Method: saturation genome editing in haploid cells
Result:
LOSS_OF_FUNCTION:-1.3708641746553
|
Comment:
Germline Functional Evidence
| Functional
Help
The functional consequence of the variant, based on experimental evidence and provided by the submitter. consequence |
Method
Help
A brief description of the method used to determine the functional consequence of the variant. A citation for the method is included, when provided by the submitter. |
Result
Help
A brief description of the result of this method for 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 functional evidence for the germline classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter. |
|---|---|---|---|---|
|
functionally_abnormal
|
Method citation(s):
|
|
Brotman Baty Institute, University of Washington
Accession: SCV001241926.1
|
Comment:
The saturation genome editing (SGE) assay for BRCA1 NM_007294.3:c.5205A>T, a MISSENSE variant, produced a function score of -1.37, corresponding to a functional classification of LOSS_OF_FUNCTION. … (more)
The saturation genome editing (SGE) assay for BRCA1 NM_007294.3:c.5205A>T, a MISSENSE variant, produced a function score of -1.37, corresponding to a functional classification of LOSS_OF_FUNCTION. SGE function score ranges for classification are as follows: ‘functional’, score > -0.748; ‘intermediate’, -0.748 > score > -1.328; ‘non-functional’, score < -1.328. The median synonymous SNV scored 0.0 and the median nonsense SNV scored -2.12. (less)
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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 of Uncertain Significance. Experimental studies have shown that this missense change affects BRCA1 function (PMID: 30209399). Advanced modeling performed at Invitae incorporating data from internal and/or published experimental studies (PMID: 30209399) indicates that this missense variant is expected to disrupt BRCA1 function. ClinVar contains an entry for this variant (Variation ID: 96943). 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 glutamic acid, which is acidic and polar, with aspartic acid, which is acidic and polar, at codon 1735 of the BRCA1 protein (p.Glu1735Asp).
Citations for germline classification of this variant
Help| Title | Author | Journal | Year | Link |
|---|---|---|---|---|
| Accurate classification of BRCA1 variants with saturation genome editing. | Findlay GM | Nature | 2018 | PMID: 30209399 |
| https://sge.gs.washington.edu/BRCA1/ | - | - | - | - |
Text-mined citations for rs431825412 ...
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Record last updated Oct 08, 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.