IARC class based on posterior probability from multifactorial likelihood analysis, thresholds for class as per Plon et al. 2008 (PMID: 18951446). Class 1 based on posterior probability = 0.0000697
ClinVar Genomic variation as it relates to human health
NM_007294.4(BRCA1):c.5572A>C (p.Ile1858Leu)
Germline
Top reviewed classifications are shown here.
Submission summary:
Reviewed by expert panel
Benign
Aug 2015 by
Evidence-based…
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Variant Details
- Identifiers
-
NM_007294.4(BRCA1):c.5572A>C (p.Ile1858Leu)
Variation ID: 183951 Accession: VCV000183951.23
- Type and length
-
single nucleotide variant, 1 bp
- Location
-
Cytogenetic: 17q21.31 17: 43045698 (GRCh38) [ NCBI UCSC ] 17: 41197715 (GRCh37) [ NCBI UCSC ]
- Timeline in ClinVar
-
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 29, 2015 Aug 18, 2024 Aug 10, 2015 - HGVS
-
... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_007294.4:c.5572A>C MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_009225.1:p.Ile1858Leu missense NM_001407571.1:c.5359A>C NP_001394500.1:p.Ile1787Leu missense NM_001407581.1:c.5638A>C NP_001394510.1:p.Ile1880Leu missense NM_001407582.1:c.5638A>C NP_001394511.1:p.Ile1880Leu missense NM_001407583.1:c.5635A>C NP_001394512.1:p.Ile1879Leu missense NM_001407585.1:c.5635A>C NP_001394514.1:p.Ile1879Leu missense NM_001407587.1:c.5635A>C NP_001394516.1:p.Ile1879Leu missense NM_001407590.1:c.5632A>C NP_001394519.1:p.Ile1878Leu missense NM_001407591.1:c.5632A>C NP_001394520.1:p.Ile1878Leu missense NM_001407593.1:c.5572A>C NP_001394522.1:p.Ile1858Leu missense NM_001407594.1:c.5572A>C NP_001394523.1:p.Ile1858Leu missense NM_001407596.1:c.5572A>C NP_001394525.1:p.Ile1858Leu missense NM_001407597.1:c.5572A>C NP_001394526.1:p.Ile1858Leu missense NM_001407598.1:c.5572A>C NP_001394527.1:p.Ile1858Leu missense NM_001407602.1:c.5572A>C NP_001394531.1:p.Ile1858Leu missense NM_001407603.1:c.5572A>C NP_001394532.1:p.Ile1858Leu missense NM_001407605.1:c.5572A>C NP_001394534.1:p.Ile1858Leu missense NM_001407610.1:c.5569A>C NP_001394539.1:p.Ile1857Leu missense NM_001407611.1:c.5569A>C NP_001394540.1:p.Ile1857Leu missense NM_001407612.1:c.5569A>C NP_001394541.1:p.Ile1857Leu missense NM_001407613.1:c.5569A>C NP_001394542.1:p.Ile1857Leu missense NM_001407614.1:c.5569A>C NP_001394543.1:p.Ile1857Leu missense NM_001407615.1:c.5569A>C NP_001394544.1:p.Ile1857Leu missense NM_001407616.1:c.5569A>C NP_001394545.1:p.Ile1857Leu missense NM_001407617.1:c.5569A>C NP_001394546.1:p.Ile1857Leu missense NM_001407618.1:c.5569A>C NP_001394547.1:p.Ile1857Leu missense NM_001407619.1:c.5569A>C NP_001394548.1:p.Ile1857Leu missense NM_001407620.1:c.5569A>C NP_001394549.1:p.Ile1857Leu missense NM_001407621.1:c.5569A>C NP_001394550.1:p.Ile1857Leu missense NM_001407622.1:c.5569A>C NP_001394551.1:p.Ile1857Leu missense NM_001407623.1:c.5569A>C NP_001394552.1:p.Ile1857Leu missense NM_001407624.1:c.5569A>C NP_001394553.1:p.Ile1857Leu missense NM_001407625.1:c.5569A>C NP_001394554.1:p.Ile1857Leu missense NM_001407626.1:c.5569A>C NP_001394555.1:p.Ile1857Leu missense NM_001407627.1:c.5566A>C NP_001394556.1:p.Ile1856Leu missense NM_001407628.1:c.5566A>C NP_001394557.1:p.Ile1856Leu missense NM_001407629.1:c.5566A>C NP_001394558.1:p.Ile1856Leu missense NM_001407630.1:c.5566A>C NP_001394559.1:p.Ile1856Leu missense NM_001407631.1:c.5566A>C NP_001394560.1:p.Ile1856Leu missense NM_001407632.1:c.5566A>C NP_001394561.1:p.Ile1856Leu missense NM_001407633.1:c.5566A>C NP_001394562.1:p.Ile1856Leu missense NM_001407634.1:c.5566A>C NP_001394563.1:p.Ile1856Leu missense NM_001407635.1:c.5566A>C NP_001394564.1:p.Ile1856Leu missense NM_001407636.1:c.5566A>C NP_001394565.1:p.Ile1856Leu missense NM_001407637.1:c.5566A>C NP_001394566.1:p.Ile1856Leu missense NM_001407638.1:c.5566A>C NP_001394567.1:p.Ile1856Leu missense NM_001407639.1:c.5566A>C NP_001394568.1:p.Ile1856Leu missense NM_001407640.1:c.5566A>C NP_001394569.1:p.Ile1856Leu missense NM_001407641.1:c.5566A>C NP_001394570.1:p.Ile1856Leu missense NM_001407642.1:c.5566A>C NP_001394571.1:p.Ile1856Leu missense NM_001407644.1:c.5563A>C NP_001394573.1:p.Ile1855Leu missense NM_001407645.1:c.5563A>C NP_001394574.1:p.Ile1855Leu missense NM_001407646.1:c.5560A>C NP_001394575.1:p.Ile1854Leu missense NM_001407647.1:c.5557A>C NP_001394576.1:p.Ile1853Leu missense NM_001407648.1:c.5515A>C NP_001394577.1:p.Ile1839Leu missense NM_001407649.1:c.5512A>C NP_001394578.1:p.Ile1838Leu missense NM_001407652.1:c.5494A>C NP_001394581.1:p.Ile1832Leu missense NM_001407653.1:c.5494A>C NP_001394582.1:p.Ile1832Leu missense NM_001407654.1:c.5494A>C NP_001394583.1:p.Ile1832Leu missense NM_001407655.1:c.5494A>C NP_001394584.1:p.Ile1832Leu missense NM_001407656.1:c.5491A>C NP_001394585.1:p.Ile1831Leu missense NM_001407657.1:c.5491A>C NP_001394586.1:p.Ile1831Leu missense NM_001407658.1:c.5491A>C NP_001394587.1:p.Ile1831Leu missense NM_001407659.1:c.5488A>C NP_001394588.1:p.Ile1830Leu missense NM_001407660.1:c.5488A>C NP_001394589.1:p.Ile1830Leu missense NM_001407661.1:c.5488A>C NP_001394590.1:p.Ile1830Leu missense NM_001407662.1:c.5488A>C NP_001394591.1:p.Ile1830Leu missense NM_001407663.1:c.5488A>C NP_001394592.1:p.Ile1830Leu missense NM_001407664.1:c.5449A>C NP_001394593.1:p.Ile1817Leu missense NM_001407665.1:c.5449A>C NP_001394594.1:p.Ile1817Leu missense NM_001407666.1:c.5449A>C NP_001394595.1:p.Ile1817Leu missense NM_001407667.1:c.5449A>C NP_001394596.1:p.Ile1817Leu missense NM_001407668.1:c.5449A>C NP_001394597.1:p.Ile1817Leu missense NM_001407669.1:c.5449A>C NP_001394598.1:p.Ile1817Leu missense NM_001407670.1:c.5446A>C NP_001394599.1:p.Ile1816Leu missense NM_001407671.1:c.5446A>C NP_001394600.1:p.Ile1816Leu missense NM_001407672.1:c.5446A>C NP_001394601.1:p.Ile1816Leu missense NM_001407673.1:c.5446A>C NP_001394602.1:p.Ile1816Leu missense NM_001407674.1:c.5446A>C NP_001394603.1:p.Ile1816Leu missense NM_001407675.1:c.5446A>C NP_001394604.1:p.Ile1816Leu missense NM_001407676.1:c.5446A>C NP_001394605.1:p.Ile1816Leu missense NM_001407677.1:c.5446A>C NP_001394606.1:p.Ile1816Leu missense NM_001407678.1:c.5446A>C NP_001394607.1:p.Ile1816Leu missense NM_001407679.1:c.5446A>C NP_001394608.1:p.Ile1816Leu missense NM_001407680.1:c.5446A>C NP_001394609.1:p.Ile1816Leu missense NM_001407681.1:c.5443A>C NP_001394610.1:p.Ile1815Leu missense NM_001407682.1:c.5443A>C NP_001394611.1:p.Ile1815Leu missense NM_001407683.1:c.5443A>C NP_001394612.1:p.Ile1815Leu missense NM_001407684.1:c.5443A>C NP_001394613.1:p.Ile1815Leu missense NM_001407685.1:c.5443A>C NP_001394614.1:p.Ile1815Leu missense NM_001407686.1:c.5443A>C NP_001394615.1:p.Ile1815Leu missense NM_001407687.1:c.5443A>C NP_001394616.1:p.Ile1815Leu missense NM_001407688.1:c.5443A>C NP_001394617.1:p.Ile1815Leu missense NM_001407689.1:c.5443A>C NP_001394618.1:p.Ile1815Leu missense NM_001407690.1:c.5440A>C NP_001394619.1:p.Ile1814Leu missense NM_001407691.1:c.5440A>C NP_001394620.1:p.Ile1814Leu missense NM_001407692.1:c.5431A>C NP_001394621.1:p.Ile1811Leu missense NM_001407694.1:c.5431A>C NP_001394623.1:p.Ile1811Leu missense NM_001407695.1:c.5431A>C NP_001394624.1:p.Ile1811Leu missense NM_001407696.1:c.5431A>C NP_001394625.1:p.Ile1811Leu missense NM_001407697.1:c.5431A>C NP_001394626.1:p.Ile1811Leu missense NM_001407698.1:c.5431A>C NP_001394627.1:p.Ile1811Leu missense NM_001407724.1:c.5431A>C NP_001394653.1:p.Ile1811Leu missense NM_001407725.1:c.5431A>C NP_001394654.1:p.Ile1811Leu missense NM_001407726.1:c.5431A>C NP_001394655.1:p.Ile1811Leu missense NM_001407727.1:c.5431A>C NP_001394656.1:p.Ile1811Leu missense NM_001407728.1:c.5431A>C NP_001394657.1:p.Ile1811Leu missense NM_001407729.1:c.5431A>C NP_001394658.1:p.Ile1811Leu missense NM_001407730.1:c.5431A>C NP_001394659.1:p.Ile1811Leu missense NM_001407731.1:c.5431A>C NP_001394660.1:p.Ile1811Leu missense NM_001407732.1:c.5428A>C NP_001394661.1:p.Ile1810Leu missense NM_001407733.1:c.5428A>C NP_001394662.1:p.Ile1810Leu missense NM_001407734.1:c.5428A>C NP_001394663.1:p.Ile1810Leu missense NM_001407735.1:c.5428A>C NP_001394664.1:p.Ile1810Leu missense NM_001407736.1:c.5428A>C NP_001394665.1:p.Ile1810Leu missense NM_001407737.1:c.5428A>C NP_001394666.1:p.Ile1810Leu missense NM_001407738.1:c.5428A>C NP_001394667.1:p.Ile1810Leu missense NM_001407739.1:c.5428A>C NP_001394668.1:p.Ile1810Leu missense NM_001407740.1:c.5428A>C NP_001394669.1:p.Ile1810Leu missense NM_001407741.1:c.5428A>C NP_001394670.1:p.Ile1810Leu missense NM_001407742.1:c.5428A>C NP_001394671.1:p.Ile1810Leu missense NM_001407743.1:c.5428A>C NP_001394672.1:p.Ile1810Leu missense NM_001407744.1:c.5428A>C NP_001394673.1:p.Ile1810Leu missense NM_001407745.1:c.5428A>C NP_001394674.1:p.Ile1810Leu missense NM_001407746.1:c.5428A>C NP_001394675.1:p.Ile1810Leu missense NM_001407747.1:c.5428A>C NP_001394676.1:p.Ile1810Leu missense NM_001407748.1:c.5428A>C NP_001394677.1:p.Ile1810Leu missense NM_001407749.1:c.5428A>C NP_001394678.1:p.Ile1810Leu missense NM_001407750.1:c.5428A>C NP_001394679.1:p.Ile1810Leu missense NM_001407751.1:c.5428A>C NP_001394680.1:p.Ile1810Leu missense NM_001407752.1:c.5428A>C NP_001394681.1:p.Ile1810Leu missense NM_001407838.1:c.5425A>C NP_001394767.1:p.Ile1809Leu missense NM_001407839.1:c.5425A>C NP_001394768.1:p.Ile1809Leu missense NM_001407841.1:c.5425A>C NP_001394770.1:p.Ile1809Leu missense NM_001407842.1:c.5425A>C NP_001394771.1:p.Ile1809Leu missense NM_001407843.1:c.5425A>C NP_001394772.1:p.Ile1809Leu missense NM_001407844.1:c.5425A>C NP_001394773.1:p.Ile1809Leu missense NM_001407845.1:c.5425A>C NP_001394774.1:p.Ile1809Leu missense NM_001407846.1:c.5425A>C NP_001394775.1:p.Ile1809Leu missense NM_001407847.1:c.5425A>C NP_001394776.1:p.Ile1809Leu missense NM_001407848.1:c.5425A>C NP_001394777.1:p.Ile1809Leu missense NM_001407849.1:c.5425A>C NP_001394778.1:p.Ile1809Leu missense NM_001407850.1:c.5425A>C NP_001394779.1:p.Ile1809Leu missense NM_001407851.1:c.5425A>C NP_001394780.1:p.Ile1809Leu missense NM_001407852.1:c.5425A>C NP_001394781.1:p.Ile1809Leu missense NM_001407853.1:c.5425A>C NP_001394782.1:p.Ile1809Leu missense NM_001407854.1:c.*86A>C NM_001407858.1:c.*86A>C NM_001407859.1:c.*86A>C NM_001407860.1:c.*86A>C NM_001407861.1:c.*86A>C NM_001407862.1:c.5371A>C NP_001394791.1:p.Ile1791Leu missense NM_001407863.1:c.5368A>C NP_001394792.1:p.Ile1790Leu missense NM_001407874.1:c.5365A>C NP_001394803.1:p.Ile1789Leu missense NM_001407875.1:c.5365A>C NP_001394804.1:p.Ile1789Leu missense NM_001407879.1:c.5362A>C NP_001394808.1:p.Ile1788Leu missense NM_001407881.1:c.5362A>C NP_001394810.1:p.Ile1788Leu missense NM_001407882.1:c.5362A>C NP_001394811.1:p.Ile1788Leu missense NM_001407884.1:c.5362A>C NP_001394813.1:p.Ile1788Leu missense NM_001407885.1:c.5362A>C NP_001394814.1:p.Ile1788Leu missense NM_001407886.1:c.5362A>C NP_001394815.1:p.Ile1788Leu missense NM_001407887.1:c.5362A>C NP_001394816.1:p.Ile1788Leu missense NM_001407889.1:c.5362A>C NP_001394818.1:p.Ile1788Leu missense NM_001407894.1:c.5359A>C NP_001394823.1:p.Ile1787Leu missense NM_001407895.1:c.5359A>C NP_001394824.1:p.Ile1787Leu missense NM_001407896.1:c.5359A>C NP_001394825.1:p.Ile1787Leu missense NM_001407897.1:c.5359A>C NP_001394826.1:p.Ile1787Leu missense NM_001407898.1:c.5359A>C NP_001394827.1:p.Ile1787Leu missense NM_001407899.1:c.5359A>C NP_001394828.1:p.Ile1787Leu missense NM_001407900.1:c.5359A>C NP_001394829.1:p.Ile1787Leu missense NM_001407902.1:c.5359A>C NP_001394831.1:p.Ile1787Leu missense NM_001407904.1:c.5359A>C NP_001394833.1:p.Ile1787Leu missense NM_001407906.1:c.5359A>C NP_001394835.1:p.Ile1787Leu missense NM_001407907.1:c.5359A>C NP_001394836.1:p.Ile1787Leu missense NM_001407908.1:c.5359A>C NP_001394837.1:p.Ile1787Leu missense NM_001407909.1:c.5359A>C NP_001394838.1:p.Ile1787Leu missense NM_001407910.1:c.5359A>C NP_001394839.1:p.Ile1787Leu missense NM_001407915.1:c.5356A>C NP_001394844.1:p.Ile1786Leu missense NM_001407916.1:c.5356A>C NP_001394845.1:p.Ile1786Leu missense NM_001407917.1:c.5356A>C NP_001394846.1:p.Ile1786Leu missense NM_001407918.1:c.5356A>C NP_001394847.1:p.Ile1786Leu missense NM_001407919.1:c.5320A>C NP_001394848.1:p.Ile1774Leu missense NM_001407920.1:c.5308A>C NP_001394849.1:p.Ile1770Leu missense NM_001407921.1:c.5308A>C NP_001394850.1:p.Ile1770Leu missense NM_001407922.1:c.5308A>C NP_001394851.1:p.Ile1770Leu missense NM_001407923.1:c.5308A>C NP_001394852.1:p.Ile1770Leu missense NM_001407924.1:c.5308A>C NP_001394853.1:p.Ile1770Leu missense NM_001407925.1:c.5308A>C NP_001394854.1:p.Ile1770Leu missense NM_001407926.1:c.5308A>C NP_001394855.1:p.Ile1770Leu missense NM_001407927.1:c.5305A>C NP_001394856.1:p.Ile1769Leu missense NM_001407928.1:c.5305A>C NP_001394857.1:p.Ile1769Leu missense NM_001407929.1:c.5305A>C NP_001394858.1:p.Ile1769Leu missense NM_001407930.1:c.5305A>C NP_001394859.1:p.Ile1769Leu missense NM_001407931.1:c.5305A>C NP_001394860.1:p.Ile1769Leu missense NM_001407932.1:c.5305A>C NP_001394861.1:p.Ile1769Leu missense NM_001407933.1:c.5305A>C NP_001394862.1:p.Ile1769Leu missense NM_001407934.1:c.5302A>C NP_001394863.1:p.Ile1768Leu missense NM_001407935.1:c.5302A>C NP_001394864.1:p.Ile1768Leu missense NM_001407936.1:c.5302A>C NP_001394865.1:p.Ile1768Leu missense NM_001407937.1:c.*86A>C NM_001407938.1:c.*86A>C NM_001407939.1:c.*86A>C NM_001407940.1:c.*86A>C NM_001407941.1:c.*86A>C NM_001407942.1:c.*86A>C NM_001407943.1:c.*86A>C NM_001407944.1:c.*86A>C NM_001407945.1:c.*86A>C NM_001407946.1:c.5239A>C NP_001394875.1:p.Ile1747Leu missense NM_001407947.1:c.5239A>C NP_001394876.1:p.Ile1747Leu missense NM_001407948.1:c.5239A>C NP_001394877.1:p.Ile1747Leu missense NM_001407949.1:c.5239A>C NP_001394878.1:p.Ile1747Leu missense NM_001407950.1:c.5236A>C NP_001394879.1:p.Ile1746Leu missense NM_001407951.1:c.5236A>C NP_001394880.1:p.Ile1746Leu missense NM_001407952.1:c.5236A>C NP_001394881.1:p.Ile1746Leu missense NM_001407953.1:c.5236A>C NP_001394882.1:p.Ile1746Leu missense NM_001407954.1:c.5236A>C NP_001394883.1:p.Ile1746Leu missense NM_001407955.1:c.5236A>C NP_001394884.1:p.Ile1746Leu missense NM_001407956.1:c.5233A>C NP_001394885.1:p.Ile1745Leu missense NM_001407957.1:c.5233A>C NP_001394886.1:p.Ile1745Leu missense NM_001407958.1:c.5233A>C NP_001394887.1:p.Ile1745Leu missense NM_001407959.1:c.5191A>C NP_001394888.1:p.Ile1731Leu missense NM_001407960.1:c.5188A>C NP_001394889.1:p.Ile1730Leu missense NM_001407962.1:c.5188A>C NP_001394891.1:p.Ile1730Leu missense NM_001407963.1:c.5185A>C NP_001394892.1:p.Ile1729Leu missense NM_001407964.1:c.5110A>C NP_001394893.1:p.Ile1704Leu missense NM_001407965.1:c.5065A>C NP_001394894.1:p.Ile1689Leu missense NM_001407966.1:c.4684A>C NP_001394895.1:p.Ile1562Leu missense NM_001407967.1:c.4681A>C NP_001394896.1:p.Ile1561Leu missense NM_001407968.1:c.2968A>C NP_001394897.1:p.Ile990Leu missense NM_001407969.1:c.2965A>C NP_001394898.1:p.Ile989Leu missense NM_001407970.1:c.2329A>C NP_001394899.1:p.Ile777Leu missense NM_001407971.1:c.2329A>C NP_001394900.1:p.Ile777Leu missense NM_001407972.1:c.2326A>C NP_001394901.1:p.Ile776Leu missense NM_001407973.1:c.2263A>C NP_001394902.1:p.Ile755Leu missense NM_001407974.1:c.2263A>C NP_001394903.1:p.Ile755Leu missense NM_001407975.1:c.2263A>C NP_001394904.1:p.Ile755Leu missense NM_001407976.1:c.2263A>C NP_001394905.1:p.Ile755Leu missense NM_001407977.1:c.2263A>C NP_001394906.1:p.Ile755Leu missense NM_001407978.1:c.2263A>C NP_001394907.1:p.Ile755Leu missense NM_001407979.1:c.2260A>C NP_001394908.1:p.Ile754Leu missense NM_001407980.1:c.2260A>C NP_001394909.1:p.Ile754Leu missense NM_001407981.1:c.2260A>C NP_001394910.1:p.Ile754Leu missense NM_001407982.1:c.2260A>C NP_001394911.1:p.Ile754Leu missense NM_001407983.1:c.2260A>C NP_001394912.1:p.Ile754Leu missense NM_001407984.1:c.2260A>C NP_001394913.1:p.Ile754Leu missense NM_001407985.1:c.2260A>C NP_001394914.1:p.Ile754Leu missense NM_001407986.1:c.2260A>C NP_001394915.1:p.Ile754Leu missense NM_001407990.1:c.2260A>C NP_001394919.1:p.Ile754Leu missense NM_001407991.1:c.2260A>C NP_001394920.1:p.Ile754Leu missense NM_001407992.1:c.2260A>C NP_001394921.1:p.Ile754Leu missense NM_001407993.1:c.2260A>C NP_001394922.1:p.Ile754Leu missense NM_001408392.1:c.2257A>C NP_001395321.1:p.Ile753Leu missense NM_001408396.1:c.2257A>C NP_001395325.1:p.Ile753Leu missense NM_001408397.1:c.2257A>C NP_001395326.1:p.Ile753Leu missense NM_001408398.1:c.2257A>C NP_001395327.1:p.Ile753Leu missense NM_001408399.1:c.2257A>C NP_001395328.1:p.Ile753Leu missense NM_001408400.1:c.2257A>C NP_001395329.1:p.Ile753Leu missense NM_001408401.1:c.2257A>C NP_001395330.1:p.Ile753Leu missense NM_001408402.1:c.2257A>C NP_001395331.1:p.Ile753Leu missense NM_001408403.1:c.2257A>C NP_001395332.1:p.Ile753Leu missense NM_001408404.1:c.2257A>C NP_001395333.1:p.Ile753Leu missense NM_001408406.1:c.2254A>C NP_001395335.1:p.Ile752Leu missense NM_001408407.1:c.2254A>C NP_001395336.1:p.Ile752Leu missense NM_001408408.1:c.2254A>C NP_001395337.1:p.Ile752Leu missense NM_001408409.1:c.2251A>C NP_001395338.1:p.Ile751Leu missense NM_001408410.1:c.2188A>C NP_001395339.1:p.Ile730Leu missense NM_001408411.1:c.2185A>C NP_001395340.1:p.Ile729Leu missense NM_001408412.1:c.2182A>C NP_001395341.1:p.Ile728Leu missense NM_001408413.1:c.2182A>C NP_001395342.1:p.Ile728Leu missense NM_001408414.1:c.2182A>C NP_001395343.1:p.Ile728Leu missense NM_001408415.1:c.2182A>C NP_001395344.1:p.Ile728Leu missense NM_001408416.1:c.2182A>C NP_001395345.1:p.Ile728Leu missense NM_001408418.1:c.2146A>C NP_001395347.1:p.Ile716Leu missense NM_001408419.1:c.2146A>C NP_001395348.1:p.Ile716Leu missense NM_001408420.1:c.2146A>C NP_001395349.1:p.Ile716Leu missense NM_001408421.1:c.2143A>C NP_001395350.1:p.Ile715Leu missense NM_001408422.1:c.2143A>C NP_001395351.1:p.Ile715Leu missense NM_001408423.1:c.2143A>C NP_001395352.1:p.Ile715Leu missense NM_001408424.1:c.2143A>C NP_001395353.1:p.Ile715Leu missense NM_001408425.1:c.2140A>C NP_001395354.1:p.Ile714Leu missense NM_001408426.1:c.2140A>C NP_001395355.1:p.Ile714Leu missense NM_001408427.1:c.2140A>C NP_001395356.1:p.Ile714Leu missense NM_001408428.1:c.2140A>C NP_001395357.1:p.Ile714Leu missense NM_001408429.1:c.2140A>C NP_001395358.1:p.Ile714Leu missense NM_001408430.1:c.2140A>C NP_001395359.1:p.Ile714Leu missense NM_001408431.1:c.2140A>C NP_001395360.1:p.Ile714Leu missense NM_001408432.1:c.2137A>C NP_001395361.1:p.Ile713Leu missense NM_001408433.1:c.2137A>C NP_001395362.1:p.Ile713Leu missense NM_001408434.1:c.2137A>C NP_001395363.1:p.Ile713Leu missense NM_001408435.1:c.2137A>C NP_001395364.1:p.Ile713Leu missense NM_001408436.1:c.2137A>C NP_001395365.1:p.Ile713Leu missense NM_001408437.1:c.2137A>C NP_001395366.1:p.Ile713Leu missense NM_001408438.1:c.2137A>C NP_001395367.1:p.Ile713Leu missense NM_001408439.1:c.2137A>C NP_001395368.1:p.Ile713Leu missense NM_001408440.1:c.2137A>C NP_001395369.1:p.Ile713Leu missense NM_001408441.1:c.2137A>C NP_001395370.1:p.Ile713Leu missense NM_001408442.1:c.2137A>C NP_001395371.1:p.Ile713Leu missense NM_001408443.1:c.2137A>C NP_001395372.1:p.Ile713Leu missense NM_001408444.1:c.2137A>C NP_001395373.1:p.Ile713Leu missense NM_001408445.1:c.2134A>C NP_001395374.1:p.Ile712Leu missense NM_001408446.1:c.2134A>C NP_001395375.1:p.Ile712Leu missense NM_001408447.1:c.2134A>C NP_001395376.1:p.Ile712Leu missense NM_001408448.1:c.2134A>C NP_001395377.1:p.Ile712Leu missense NM_001408450.1:c.2134A>C NP_001395379.1:p.Ile712Leu missense NM_001408451.1:c.2128A>C NP_001395380.1:p.Ile710Leu missense NM_001408452.1:c.2122A>C NP_001395381.1:p.Ile708Leu missense NM_001408453.1:c.2122A>C NP_001395382.1:p.Ile708Leu missense NM_001408454.1:c.2122A>C NP_001395383.1:p.Ile708Leu missense NM_001408455.1:c.2122A>C NP_001395384.1:p.Ile708Leu missense NM_001408456.1:c.2122A>C NP_001395385.1:p.Ile708Leu missense NM_001408457.1:c.2122A>C NP_001395386.1:p.Ile708Leu missense NM_001408458.1:c.2119A>C NP_001395387.1:p.Ile707Leu missense NM_001408459.1:c.2119A>C NP_001395388.1:p.Ile707Leu missense NM_001408460.1:c.2119A>C NP_001395389.1:p.Ile707Leu missense NM_001408461.1:c.2119A>C NP_001395390.1:p.Ile707Leu missense NM_001408462.1:c.2119A>C NP_001395391.1:p.Ile707Leu missense NM_001408463.1:c.2119A>C NP_001395392.1:p.Ile707Leu missense NM_001408464.1:c.2119A>C NP_001395393.1:p.Ile707Leu missense NM_001408465.1:c.2119A>C NP_001395394.1:p.Ile707Leu missense NM_001408466.1:c.2119A>C NP_001395395.1:p.Ile707Leu missense NM_001408467.1:c.2119A>C NP_001395396.1:p.Ile707Leu missense NM_001408468.1:c.2116A>C NP_001395397.1:p.Ile706Leu missense NM_001408469.1:c.2116A>C NP_001395398.1:p.Ile706Leu missense NM_001408470.1:c.2116A>C NP_001395399.1:p.Ile706Leu missense NM_001408472.1:c.*86A>C NM_001408473.1:c.*86A>C NM_001408474.1:c.2062A>C NP_001395403.1:p.Ile688Leu missense NM_001408475.1:c.2059A>C NP_001395404.1:p.Ile687Leu missense NM_001408476.1:c.2059A>C NP_001395405.1:p.Ile687Leu missense NM_001408478.1:c.2053A>C NP_001395407.1:p.Ile685Leu missense NM_001408479.1:c.2053A>C NP_001395408.1:p.Ile685Leu missense NM_001408480.1:c.2053A>C NP_001395409.1:p.Ile685Leu missense NM_001408481.1:c.2050A>C NP_001395410.1:p.Ile684Leu missense NM_001408482.1:c.2050A>C NP_001395411.1:p.Ile684Leu missense NM_001408483.1:c.2050A>C NP_001395412.1:p.Ile684Leu missense NM_001408484.1:c.2050A>C NP_001395413.1:p.Ile684Leu missense NM_001408485.1:c.2050A>C NP_001395414.1:p.Ile684Leu missense NM_001408489.1:c.2050A>C NP_001395418.1:p.Ile684Leu missense NM_001408490.1:c.2050A>C NP_001395419.1:p.Ile684Leu missense NM_001408491.1:c.2050A>C NP_001395420.1:p.Ile684Leu missense NM_001408492.1:c.2047A>C NP_001395421.1:p.Ile683Leu missense NM_001408493.1:c.2047A>C NP_001395422.1:p.Ile683Leu missense NM_001408494.1:c.2023A>C NP_001395423.1:p.Ile675Leu missense NM_001408495.1:c.2017A>C NP_001395424.1:p.Ile673Leu missense NM_001408496.1:c.1999A>C NP_001395425.1:p.Ile667Leu missense NM_001408497.1:c.1999A>C NP_001395426.1:p.Ile667Leu missense NM_001408498.1:c.1999A>C NP_001395427.1:p.Ile667Leu missense NM_001408499.1:c.1999A>C NP_001395428.1:p.Ile667Leu missense NM_001408500.1:c.1999A>C NP_001395429.1:p.Ile667Leu missense NM_001408501.1:c.1999A>C NP_001395430.1:p.Ile667Leu missense NM_001408502.1:c.1996A>C NP_001395431.1:p.Ile666Leu missense NM_001408503.1:c.1996A>C NP_001395432.1:p.Ile666Leu missense NM_001408504.1:c.1996A>C NP_001395433.1:p.Ile666Leu missense NM_001408505.1:c.1993A>C NP_001395434.1:p.Ile665Leu missense NM_001408506.1:c.1936A>C NP_001395435.1:p.Ile646Leu missense NM_001408507.1:c.1933A>C NP_001395436.1:p.Ile645Leu missense NM_001408508.1:c.1924A>C NP_001395437.1:p.Ile642Leu missense NM_001408509.1:c.1921A>C NP_001395438.1:p.Ile641Leu missense NM_001408510.1:c.1882A>C NP_001395439.1:p.Ile628Leu missense NM_001408511.1:c.1879A>C NP_001395440.1:p.Ile627Leu missense NM_001408512.1:c.1759A>C NP_001395441.1:p.Ile587Leu missense NM_001408513.1:c.1732A>C NP_001395442.1:p.Ile578Leu missense NM_001408514.1:c.1336A>C NP_001395443.1:p.Ile446Leu missense NM_007297.4:c.5431A>C NP_009228.2:p.Ile1811Leu missense NM_007298.4:c.2260A>C NP_009229.2:p.Ile754Leu missense NM_007299.4:c.*86A>C 3 prime UTR NM_007300.4:c.5635A>C NP_009231.2:p.Ile1879Leu missense NM_007304.2:c.2260A>C NP_009235.2:p.Ile754Leu missense NR_027676.2:n.5749A>C non-coding transcript variant NC_000017.11:g.43045698T>G NC_000017.10:g.41197715T>G NG_005905.2:g.172286A>C LRG_292:g.172286A>C LRG_292t1:c.5572A>C LRG_292p1:p.Ile1858Leu - Protein change
- I1858L, I1879L, I1811L, I754L, I1561L, I1562L, I1730L, I1745L, I1786L, I1789L, I1830L, I1831L, I1856L, I1857L, I1880L, I578L, I666L, I675L, I685L, I688L, I713L, I716L, I729L, I753L, I777L, I989L, I1689L, I1731L, I1747L, I1774L, I1788L, I1809L, I1810L, I1814L, I1832L, I1838L, I1839L, I446L, I628L, I645L, I667L, I673L, I687L, I706L, I707L, I708L, I715L, I751L, I752L, I776L, I642L, I683L, I710L, I714L, I728L, I755L, I1704L, I1787L, I1815L, I1817L, I1853L, I1854L, I1878L, I1729L, I1746L, I1768L, I1769L, I1770L, I1790L, I1791L, I1816L, I1855L, I587L, I627L, I641L, I646L, I665L, I684L, I712L, I730L, I990L
- Other names
-
5691A>C
- Canonical SPDI
- NC_000017.11:43045697:T:G
-
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.
-
The Genome Aggregation Database (gnomAD) 0.00000
Exome Aggregation Consortium (ExAC) 0.00006
The Genome Aggregation Database (gnomAD), exomes 0.00006
1000 Genomes Project 30x 0.00016
- 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. |
|---|---|---|---|---|
| Benign/Likely benign (3) |
criteria provided, multiple submitters, no conflicts
|
Jun 2, 2021 | RCV000162994.15 | |
| Benign (3) |
reviewed by expert panel
|
Aug 10, 2015 | RCV000191157.12 | |
| Benign/Likely benign (3) |
criteria provided, multiple submitters, no conflicts
|
Jul 11, 2022 | RCV000445348.12 | |
| Benign (1) |
criteria provided, single submitter
|
Dec 27, 2023 | RCV001085714.16 | |
|
NICE approved PARP inhibitor treatment
|
Benign (1) |
criteria provided, single submitter
|
May 9, 2024 | RCV004692770.1 |
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. |
|
|---|---|---|---|---|---|
|
Benign
(Aug 10, 2015)
|
reviewed by expert panel
Method: curation
|
Breast-ovarian cancer, familial 1
Affected status: unknown
Allele origin:
germline
|
Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA)
Accession: SCV000244405.1
First in ClinVar: Sep 29, 2015 Last updated: Sep 29, 2015 |
Comment:
IARC class based on posterior probability from multifactorial likelihood analysis, thresholds for class as per Plon et al. 2008 (PMID: 18951446). Class 1 based on … (more)
IARC class based on posterior probability from multifactorial likelihood analysis, thresholds for class as per Plon et al. 2008 (PMID: 18951446). Class 1 based on posterior probability = 0.0000697 (less)
|
|
|
Benign
(Nov 22, 2019)
|
criteria provided, single submitter
Method: clinical testing
|
not specified
Affected status: unknown
Allele origin:
unknown
|
Quest Diagnostics Nichols Institute San Juan Capistrano
Accession: SCV000888953.2
First in ClinVar: Mar 17, 2018 Last updated: Jan 26, 2021 |
|
|
|
Benign
(Jul 11, 2022)
|
criteria provided, single submitter
Method: clinical testing
|
not specified
Affected status: unknown
Allele origin:
germline
|
Women's Health and Genetics/Laboratory Corporation of America, LabCorp
Accession: SCV000699274.2
First in ClinVar: Mar 17, 2018 Last updated: Sep 17, 2022 |
Comment:
Variant summary: BRCA1 c.5572A>C (p.Ile1858Leu) results in a conservative amino acid change in the encoded protein sequence. Four of five in-silico tools predict a benign … (more)
Variant summary: BRCA1 c.5572A>C (p.Ile1858Leu) results in a conservative amino acid change in the encoded protein sequence. Four of five in-silico tools predict a benign effect of the variant on protein function. The variant allele was found at a frequency of 6.4e-05 in 250816 control chromosomes. This frequency is not significantly higher than expected for a pathogenic variant in BRCA1 causing Hereditary Breast And Ovarian Cancer Syndrome (6.4e-05 vs 0.001), allowing no conclusion about variant significance. At least two publications report experimental evidence evaluating an impact on protein function. These results showed no damaging effect of this variant (Woods_2016, Thouvenot_2016). Seven other clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014 without evidence for independent evaluation. All laboratories classified the variant as benign (n=4)/likely benign (n=3). Based on the evidence outlined above, the variant was classified as benign. (less)
|
|
|
Benign
(Dec 08, 2015)
|
criteria provided, single submitter
Method: clinical testing
|
Breast-ovarian cancer, familial, susceptibility to, 1
Affected status: unknown
Allele origin:
unknown
|
Counsyl
Accession: SCV000487900.2
First in ClinVar: Sep 29, 2015 Last updated: Dec 24, 2022 |
|
|
|
Benign
(Dec 27, 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: SCV000549368.9
First in ClinVar: Apr 17, 2017 Last updated: Feb 20, 2024 |
|
|
|
Likely Benign
(Apr 10, 2023)
|
criteria provided, single submitter
Method: clinical testing
|
Breast-ovarian cancer, familial, susceptibility to, 1
(Autosomal dominant inheritance)
Affected status: unknown
Allele origin:
germline
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All of Us Research Program, National Institutes of Health
Accession: SCV004817525.1
First in ClinVar: Apr 20, 2024 Last updated: Apr 20, 2024
Comment:
This study involves interpretation of variants in research participants for the purpose of population health screening. Participant phenotype was not available at the time of … (more)
This study involves interpretation of variants in research participants for the purpose of population health screening. Participant phenotype was not available at the time of variant classification. Additional details can be found in publication PMID: 35346344, PMCID: PMC8962531 (less)
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Number of individuals with the variant: 2
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Benign
(Nov 18, 2014)
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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: SCV000213482.6
First in ClinVar: Mar 24, 2015 Last updated: May 01, 2024 |
Comment:
This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation … (more)
This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. (less)
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Benign
(May 09, 2024)
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criteria provided, single submitter
Method: clinical testing
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NICE approved PARP inhibitor treatment
Affected status: yes
Allele origin:
germline
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Genomics and Molecular Medicine Service, East Genomic Laboratory Hub, NHS Genomic Medicine Service
Accession: SCV005196374.1
First in ClinVar: Aug 18, 2024 Last updated: Aug 18, 2024 |
Comment:
BS1_Strong,BP1,BP5_Very Strong
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Likely benign
(Jan 31, 2018)
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criteria provided, single submitter
Method: clinical testing
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not specified
Affected status: yes
Allele origin:
germline
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GeneDx
Accession: SCV000512323.4
First in ClinVar: Mar 08, 2017 Last updated: Apr 09, 2018 |
Comment:
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at … (more)
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. (less)
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Likely benign
(Jun 02, 2021)
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criteria provided, single submitter
Method: curation
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Hereditary cancer-predisposing syndrome
Affected status: unknown
Allele origin:
germline
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Sema4, Sema4
Accession: SCV002537872.1
First in ClinVar: Mar 25, 2020 Last updated: Mar 25, 2020 |
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Likely benign
(Sep 22, 2017)
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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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Color Diagnostics, LLC DBA Color Health
Accession: SCV000688643.2
First in ClinVar: Feb 19, 2018 Last updated: Dec 11, 2022 |
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Comment:
Comment:
Variant summary: BRCA1 c.5572A>C (p.Ile1858Leu) results in a conservative amino acid change in the encoded protein sequence. Four of five in-silico tools predict a benign effect of the variant on protein function. The variant allele was found at a frequency of 6.4e-05 in 250816 control chromosomes. This frequency is not significantly higher than expected for a pathogenic variant in BRCA1 causing Hereditary Breast And Ovarian Cancer Syndrome (6.4e-05 vs 0.001), allowing no conclusion about variant significance. At least two publications report experimental evidence evaluating an impact on protein function. These results showed no damaging effect of this variant (Woods_2016, Thouvenot_2016). Seven other clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014 without evidence for independent evaluation. All laboratories classified the variant as benign (n=4)/likely benign (n=3). Based on the evidence outlined above, the variant was classified as benign.
Comment:
This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Comment:
BS1_Strong,BP1,BP5_Very Strong
Comment:
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
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. |
Comment:
IARC class based on posterior probability from multifactorial likelihood analysis, thresholds for class as per Plon et al. 2008 (PMID: 18951446). Class 1 based on posterior probability = 0.0000697
Comment:
Variant summary: BRCA1 c.5572A>C (p.Ile1858Leu) results in a conservative amino acid change in the encoded protein sequence. Four of five in-silico tools predict a benign effect of the variant on protein function. The variant allele was found at a frequency of 6.4e-05 in 250816 control chromosomes. This frequency is not significantly higher than expected for a pathogenic variant in BRCA1 causing Hereditary Breast And Ovarian Cancer Syndrome (6.4e-05 vs 0.001), allowing no conclusion about variant significance. At least two publications report experimental evidence evaluating an impact on protein function. These results showed no damaging effect of this variant (Woods_2016, Thouvenot_2016). Seven other clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014 without evidence for independent evaluation. All laboratories classified the variant as benign (n=4)/likely benign (n=3). Based on the evidence outlined above, the variant was classified as benign.
Comment:
This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Comment:
BS1_Strong,BP1,BP5_Very Strong
Comment:
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Citations for germline classification of this variant
Help| Title | Author | Journal | Year | Link |
|---|---|---|---|---|
| Functional assays provide a robust tool for the clinical annotation of genetic variants of uncertain significance. | Woods NT | NPJ genomic medicine | 2016 | PMID: 28781887 |
| Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making. | Thouvenot P | PLoS genetics | 2016 | PMID: 27272900 |
| Benchmarking mutation effect prediction algorithms using functionally validated cancer-related missense mutations. | Martelotto LG | Genome biology | 2014 | PMID: 25348012 |
| A guide for functional analysis of BRCA1 variants of uncertain significance. | Millot GA | Human mutation | 2012 | PMID: 22753008 |
| BRCA1/BRCA2 gene mutations/SNPs and BRCA1 haplotypes in early-onset breast cancer patients of Indian ethnicity. | Juwle A | Medical oncology (Northwood, London, England) | 2012 | PMID: 22752604 |
| A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS). | Lindor NM | Human mutation | 2012 | PMID: 21990134 |
| A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes. | Easton DF | American journal of human genetics | 2007 | PMID: 17924331 |
| http://hci-exlovd.hci.utah.edu/variants.php?select_db=BRCA1&action=search_all&search_Variant%2FDNA=c.5572A%3EC | - | - | - | - |
Text-mined citations for rs765656957 ...
HelpThese citations are identified by LitVar using
the rs number, so they may include citations for more than one variant
at this location. Please review the LitVar results carefully for your
variant of interest.
Record last updated Nov 10, 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.