ClinVar Genomic variation as it relates to human health
NM_007294.4(BRCA1):c.5574C>G (p.Ile1858Met)
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.
No data submitted for somatic clinical impact
No data submitted for oncogenicity
Variant Details
- Identifiers
-
NM_007294.4(BRCA1):c.5574C>G (p.Ile1858Met)
Variation ID: 438943 Accession: VCV000438943.19
- Type and length
-
single nucleotide variant, 1 bp
- Location
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Cytogenetic: 17q21.31 17: 43045696 (GRCh38) [ NCBI UCSC ] 17: 41197713 (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 30, 2017 May 1, 2024 Jun 13, 2023 - HGVS
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Nucleotide Protein Molecular
consequenceNM_007294.4:c.5574C>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_009225.1:p.Ile1858Met missense NM_001407571.1:c.5361C>G NP_001394500.1:p.Ile1787Met missense NM_001407581.1:c.5640C>G NP_001394510.1:p.Ile1880Met missense NM_001407582.1:c.5640C>G NP_001394511.1:p.Ile1880Met missense NM_001407583.1:c.5637C>G NP_001394512.1:p.Ile1879Met missense NM_001407585.1:c.5637C>G NP_001394514.1:p.Ile1879Met missense NM_001407587.1:c.5637C>G NP_001394516.1:p.Ile1879Met missense NM_001407590.1:c.5634C>G NP_001394519.1:p.Ile1878Met missense NM_001407591.1:c.5634C>G NP_001394520.1:p.Ile1878Met missense NM_001407593.1:c.5574C>G NP_001394522.1:p.Ile1858Met missense NM_001407594.1:c.5574C>G NP_001394523.1:p.Ile1858Met missense NM_001407596.1:c.5574C>G NP_001394525.1:p.Ile1858Met missense NM_001407597.1:c.5574C>G NP_001394526.1:p.Ile1858Met missense NM_001407598.1:c.5574C>G NP_001394527.1:p.Ile1858Met missense NM_001407602.1:c.5574C>G NP_001394531.1:p.Ile1858Met missense NM_001407603.1:c.5574C>G NP_001394532.1:p.Ile1858Met missense NM_001407605.1:c.5574C>G NP_001394534.1:p.Ile1858Met missense NM_001407610.1:c.5571C>G NP_001394539.1:p.Ile1857Met missense NM_001407611.1:c.5571C>G NP_001394540.1:p.Ile1857Met missense NM_001407612.1:c.5571C>G NP_001394541.1:p.Ile1857Met missense NM_001407613.1:c.5571C>G NP_001394542.1:p.Ile1857Met missense NM_001407614.1:c.5571C>G NP_001394543.1:p.Ile1857Met missense NM_001407615.1:c.5571C>G NP_001394544.1:p.Ile1857Met missense NM_001407616.1:c.5571C>G NP_001394545.1:p.Ile1857Met missense NM_001407617.1:c.5571C>G NP_001394546.1:p.Ile1857Met missense NM_001407618.1:c.5571C>G NP_001394547.1:p.Ile1857Met missense NM_001407619.1:c.5571C>G NP_001394548.1:p.Ile1857Met missense NM_001407620.1:c.5571C>G NP_001394549.1:p.Ile1857Met missense NM_001407621.1:c.5571C>G NP_001394550.1:p.Ile1857Met missense NM_001407622.1:c.5571C>G NP_001394551.1:p.Ile1857Met missense NM_001407623.1:c.5571C>G NP_001394552.1:p.Ile1857Met missense NM_001407624.1:c.5571C>G NP_001394553.1:p.Ile1857Met missense NM_001407625.1:c.5571C>G NP_001394554.1:p.Ile1857Met missense NM_001407626.1:c.5571C>G NP_001394555.1:p.Ile1857Met missense NM_001407627.1:c.5568C>G NP_001394556.1:p.Ile1856Met missense NM_001407628.1:c.5568C>G NP_001394557.1:p.Ile1856Met missense NM_001407629.1:c.5568C>G NP_001394558.1:p.Ile1856Met missense NM_001407630.1:c.5568C>G NP_001394559.1:p.Ile1856Met missense NM_001407631.1:c.5568C>G NP_001394560.1:p.Ile1856Met missense NM_001407632.1:c.5568C>G NP_001394561.1:p.Ile1856Met missense NM_001407633.1:c.5568C>G NP_001394562.1:p.Ile1856Met missense NM_001407634.1:c.5568C>G NP_001394563.1:p.Ile1856Met missense NM_001407635.1:c.5568C>G NP_001394564.1:p.Ile1856Met missense NM_001407636.1:c.5568C>G NP_001394565.1:p.Ile1856Met missense NM_001407637.1:c.5568C>G NP_001394566.1:p.Ile1856Met missense NM_001407638.1:c.5568C>G NP_001394567.1:p.Ile1856Met missense NM_001407639.1:c.5568C>G NP_001394568.1:p.Ile1856Met missense NM_001407640.1:c.5568C>G NP_001394569.1:p.Ile1856Met missense NM_001407641.1:c.5568C>G NP_001394570.1:p.Ile1856Met missense NM_001407642.1:c.5568C>G NP_001394571.1:p.Ile1856Met missense NM_001407644.1:c.5565C>G NP_001394573.1:p.Ile1855Met missense NM_001407645.1:c.5565C>G NP_001394574.1:p.Ile1855Met missense NM_001407646.1:c.5562C>G NP_001394575.1:p.Ile1854Met missense NM_001407647.1:c.5559C>G NP_001394576.1:p.Ile1853Met missense NM_001407648.1:c.5517C>G NP_001394577.1:p.Ile1839Met missense NM_001407649.1:c.5514C>G NP_001394578.1:p.Ile1838Met missense NM_001407652.1:c.5496C>G NP_001394581.1:p.Ile1832Met missense NM_001407653.1:c.5496C>G NP_001394582.1:p.Ile1832Met missense NM_001407654.1:c.5496C>G NP_001394583.1:p.Ile1832Met missense NM_001407655.1:c.5496C>G NP_001394584.1:p.Ile1832Met missense NM_001407656.1:c.5493C>G NP_001394585.1:p.Ile1831Met missense NM_001407657.1:c.5493C>G NP_001394586.1:p.Ile1831Met missense NM_001407658.1:c.5493C>G NP_001394587.1:p.Ile1831Met missense NM_001407659.1:c.5490C>G NP_001394588.1:p.Ile1830Met missense NM_001407660.1:c.5490C>G NP_001394589.1:p.Ile1830Met missense NM_001407661.1:c.5490C>G NP_001394590.1:p.Ile1830Met missense NM_001407662.1:c.5490C>G NP_001394591.1:p.Ile1830Met missense NM_001407663.1:c.5490C>G NP_001394592.1:p.Ile1830Met missense NM_001407664.1:c.5451C>G NP_001394593.1:p.Ile1817Met missense NM_001407665.1:c.5451C>G NP_001394594.1:p.Ile1817Met missense NM_001407666.1:c.5451C>G NP_001394595.1:p.Ile1817Met missense NM_001407667.1:c.5451C>G NP_001394596.1:p.Ile1817Met missense NM_001407668.1:c.5451C>G NP_001394597.1:p.Ile1817Met missense NM_001407669.1:c.5451C>G NP_001394598.1:p.Ile1817Met missense NM_001407670.1:c.5448C>G NP_001394599.1:p.Ile1816Met missense NM_001407671.1:c.5448C>G NP_001394600.1:p.Ile1816Met missense NM_001407672.1:c.5448C>G NP_001394601.1:p.Ile1816Met missense NM_001407673.1:c.5448C>G NP_001394602.1:p.Ile1816Met missense NM_001407674.1:c.5448C>G NP_001394603.1:p.Ile1816Met missense NM_001407675.1:c.5448C>G NP_001394604.1:p.Ile1816Met missense NM_001407676.1:c.5448C>G NP_001394605.1:p.Ile1816Met missense NM_001407677.1:c.5448C>G NP_001394606.1:p.Ile1816Met missense NM_001407678.1:c.5448C>G NP_001394607.1:p.Ile1816Met missense NM_001407679.1:c.5448C>G NP_001394608.1:p.Ile1816Met missense NM_001407680.1:c.5448C>G NP_001394609.1:p.Ile1816Met missense NM_001407681.1:c.5445C>G NP_001394610.1:p.Ile1815Met missense NM_001407682.1:c.5445C>G NP_001394611.1:p.Ile1815Met missense NM_001407683.1:c.5445C>G NP_001394612.1:p.Ile1815Met missense NM_001407684.1:c.5445C>G NP_001394613.1:p.Ile1815Met missense NM_001407685.1:c.5445C>G NP_001394614.1:p.Ile1815Met missense NM_001407686.1:c.5445C>G NP_001394615.1:p.Ile1815Met missense NM_001407687.1:c.5445C>G NP_001394616.1:p.Ile1815Met missense NM_001407688.1:c.5445C>G NP_001394617.1:p.Ile1815Met missense NM_001407689.1:c.5445C>G NP_001394618.1:p.Ile1815Met missense NM_001407690.1:c.5442C>G NP_001394619.1:p.Ile1814Met missense NM_001407691.1:c.5442C>G NP_001394620.1:p.Ile1814Met missense NM_001407692.1:c.5433C>G NP_001394621.1:p.Ile1811Met missense NM_001407694.1:c.5433C>G NP_001394623.1:p.Ile1811Met missense NM_001407695.1:c.5433C>G NP_001394624.1:p.Ile1811Met missense NM_001407696.1:c.5433C>G NP_001394625.1:p.Ile1811Met missense NM_001407697.1:c.5433C>G NP_001394626.1:p.Ile1811Met missense NM_001407698.1:c.5433C>G NP_001394627.1:p.Ile1811Met missense NM_001407724.1:c.5433C>G NP_001394653.1:p.Ile1811Met missense NM_001407725.1:c.5433C>G NP_001394654.1:p.Ile1811Met missense NM_001407726.1:c.5433C>G NP_001394655.1:p.Ile1811Met missense NM_001407727.1:c.5433C>G NP_001394656.1:p.Ile1811Met missense NM_001407728.1:c.5433C>G NP_001394657.1:p.Ile1811Met missense NM_001407729.1:c.5433C>G NP_001394658.1:p.Ile1811Met missense NM_001407730.1:c.5433C>G NP_001394659.1:p.Ile1811Met missense NM_001407731.1:c.5433C>G NP_001394660.1:p.Ile1811Met missense NM_001407732.1:c.5430C>G NP_001394661.1:p.Ile1810Met missense NM_001407733.1:c.5430C>G NP_001394662.1:p.Ile1810Met missense NM_001407734.1:c.5430C>G NP_001394663.1:p.Ile1810Met missense NM_001407735.1:c.5430C>G NP_001394664.1:p.Ile1810Met missense NM_001407736.1:c.5430C>G NP_001394665.1:p.Ile1810Met missense NM_001407737.1:c.5430C>G NP_001394666.1:p.Ile1810Met missense NM_001407738.1:c.5430C>G NP_001394667.1:p.Ile1810Met missense NM_001407739.1:c.5430C>G NP_001394668.1:p.Ile1810Met missense NM_001407740.1:c.5430C>G NP_001394669.1:p.Ile1810Met missense NM_001407741.1:c.5430C>G NP_001394670.1:p.Ile1810Met missense NM_001407742.1:c.5430C>G NP_001394671.1:p.Ile1810Met missense NM_001407743.1:c.5430C>G NP_001394672.1:p.Ile1810Met missense NM_001407744.1:c.5430C>G NP_001394673.1:p.Ile1810Met missense NM_001407745.1:c.5430C>G NP_001394674.1:p.Ile1810Met missense NM_001407746.1:c.5430C>G NP_001394675.1:p.Ile1810Met missense NM_001407747.1:c.5430C>G NP_001394676.1:p.Ile1810Met missense NM_001407748.1:c.5430C>G NP_001394677.1:p.Ile1810Met missense NM_001407749.1:c.5430C>G NP_001394678.1:p.Ile1810Met missense NM_001407750.1:c.5430C>G NP_001394679.1:p.Ile1810Met missense NM_001407751.1:c.5430C>G NP_001394680.1:p.Ile1810Met missense NM_001407752.1:c.5430C>G NP_001394681.1:p.Ile1810Met missense NM_001407838.1:c.5427C>G NP_001394767.1:p.Ile1809Met missense NM_001407839.1:c.5427C>G NP_001394768.1:p.Ile1809Met missense NM_001407841.1:c.5427C>G NP_001394770.1:p.Ile1809Met missense NM_001407842.1:c.5427C>G NP_001394771.1:p.Ile1809Met missense NM_001407843.1:c.5427C>G NP_001394772.1:p.Ile1809Met missense NM_001407844.1:c.5427C>G NP_001394773.1:p.Ile1809Met missense NM_001407845.1:c.5427C>G NP_001394774.1:p.Ile1809Met missense NM_001407846.1:c.5427C>G NP_001394775.1:p.Ile1809Met missense NM_001407847.1:c.5427C>G NP_001394776.1:p.Ile1809Met missense NM_001407848.1:c.5427C>G NP_001394777.1:p.Ile1809Met missense NM_001407849.1:c.5427C>G NP_001394778.1:p.Ile1809Met missense NM_001407850.1:c.5427C>G NP_001394779.1:p.Ile1809Met missense NM_001407851.1:c.5427C>G NP_001394780.1:p.Ile1809Met missense NM_001407852.1:c.5427C>G NP_001394781.1:p.Ile1809Met missense NM_001407853.1:c.5427C>G NP_001394782.1:p.Ile1809Met missense NM_001407854.1:c.*88C>G NM_001407858.1:c.*88C>G NM_001407859.1:c.*88C>G NM_001407860.1:c.*88C>G NM_001407861.1:c.*88C>G NM_001407862.1:c.5373C>G NP_001394791.1:p.Ile1791Met missense NM_001407863.1:c.5370C>G NP_001394792.1:p.Ile1790Met missense NM_001407874.1:c.5367C>G NP_001394803.1:p.Ile1789Met missense NM_001407875.1:c.5367C>G NP_001394804.1:p.Ile1789Met missense NM_001407879.1:c.5364C>G NP_001394808.1:p.Ile1788Met missense NM_001407881.1:c.5364C>G NP_001394810.1:p.Ile1788Met missense NM_001407882.1:c.5364C>G NP_001394811.1:p.Ile1788Met missense NM_001407884.1:c.5364C>G NP_001394813.1:p.Ile1788Met missense NM_001407885.1:c.5364C>G NP_001394814.1:p.Ile1788Met missense NM_001407886.1:c.5364C>G NP_001394815.1:p.Ile1788Met missense NM_001407887.1:c.5364C>G NP_001394816.1:p.Ile1788Met missense NM_001407889.1:c.5364C>G NP_001394818.1:p.Ile1788Met missense NM_001407894.1:c.5361C>G NP_001394823.1:p.Ile1787Met missense NM_001407895.1:c.5361C>G NP_001394824.1:p.Ile1787Met missense NM_001407896.1:c.5361C>G NP_001394825.1:p.Ile1787Met missense NM_001407897.1:c.5361C>G NP_001394826.1:p.Ile1787Met missense NM_001407898.1:c.5361C>G NP_001394827.1:p.Ile1787Met missense NM_001407899.1:c.5361C>G NP_001394828.1:p.Ile1787Met missense NM_001407900.1:c.5361C>G NP_001394829.1:p.Ile1787Met missense NM_001407902.1:c.5361C>G NP_001394831.1:p.Ile1787Met missense NM_001407904.1:c.5361C>G NP_001394833.1:p.Ile1787Met missense NM_001407906.1:c.5361C>G NP_001394835.1:p.Ile1787Met missense NM_001407907.1:c.5361C>G NP_001394836.1:p.Ile1787Met missense NM_001407908.1:c.5361C>G NP_001394837.1:p.Ile1787Met missense NM_001407909.1:c.5361C>G NP_001394838.1:p.Ile1787Met missense NM_001407910.1:c.5361C>G NP_001394839.1:p.Ile1787Met missense NM_001407915.1:c.5358C>G NP_001394844.1:p.Ile1786Met missense NM_001407916.1:c.5358C>G NP_001394845.1:p.Ile1786Met missense NM_001407917.1:c.5358C>G NP_001394846.1:p.Ile1786Met missense NM_001407918.1:c.5358C>G NP_001394847.1:p.Ile1786Met missense NM_001407919.1:c.5322C>G NP_001394848.1:p.Ile1774Met missense NM_001407920.1:c.5310C>G NP_001394849.1:p.Ile1770Met missense NM_001407921.1:c.5310C>G NP_001394850.1:p.Ile1770Met missense NM_001407922.1:c.5310C>G NP_001394851.1:p.Ile1770Met missense NM_001407923.1:c.5310C>G NP_001394852.1:p.Ile1770Met missense NM_001407924.1:c.5310C>G NP_001394853.1:p.Ile1770Met missense NM_001407925.1:c.5310C>G NP_001394854.1:p.Ile1770Met missense NM_001407926.1:c.5310C>G NP_001394855.1:p.Ile1770Met missense NM_001407927.1:c.5307C>G NP_001394856.1:p.Ile1769Met missense NM_001407928.1:c.5307C>G NP_001394857.1:p.Ile1769Met missense NM_001407929.1:c.5307C>G NP_001394858.1:p.Ile1769Met missense NM_001407930.1:c.5307C>G NP_001394859.1:p.Ile1769Met missense NM_001407931.1:c.5307C>G NP_001394860.1:p.Ile1769Met missense NM_001407932.1:c.5307C>G NP_001394861.1:p.Ile1769Met missense NM_001407933.1:c.5307C>G NP_001394862.1:p.Ile1769Met missense NM_001407934.1:c.5304C>G NP_001394863.1:p.Ile1768Met missense NM_001407935.1:c.5304C>G NP_001394864.1:p.Ile1768Met missense NM_001407936.1:c.5304C>G NP_001394865.1:p.Ile1768Met missense NM_001407937.1:c.*88C>G NM_001407938.1:c.*88C>G NM_001407939.1:c.*88C>G NM_001407940.1:c.*88C>G NM_001407941.1:c.*88C>G NM_001407942.1:c.*88C>G NM_001407943.1:c.*88C>G NM_001407944.1:c.*88C>G NM_001407945.1:c.*88C>G NM_001407946.1:c.5241C>G NP_001394875.1:p.Ile1747Met missense NM_001407947.1:c.5241C>G NP_001394876.1:p.Ile1747Met missense NM_001407948.1:c.5241C>G NP_001394877.1:p.Ile1747Met missense NM_001407949.1:c.5241C>G NP_001394878.1:p.Ile1747Met missense NM_001407950.1:c.5238C>G NP_001394879.1:p.Ile1746Met missense NM_001407951.1:c.5238C>G NP_001394880.1:p.Ile1746Met missense NM_001407952.1:c.5238C>G NP_001394881.1:p.Ile1746Met missense NM_001407953.1:c.5238C>G NP_001394882.1:p.Ile1746Met missense NM_001407954.1:c.5238C>G NP_001394883.1:p.Ile1746Met missense NM_001407955.1:c.5238C>G NP_001394884.1:p.Ile1746Met missense NM_001407956.1:c.5235C>G NP_001394885.1:p.Ile1745Met missense NM_001407957.1:c.5235C>G NP_001394886.1:p.Ile1745Met missense NM_001407958.1:c.5235C>G NP_001394887.1:p.Ile1745Met missense NM_001407959.1:c.5193C>G NP_001394888.1:p.Ile1731Met missense NM_001407960.1:c.5190C>G NP_001394889.1:p.Ile1730Met missense NM_001407962.1:c.5190C>G NP_001394891.1:p.Ile1730Met missense NM_001407963.1:c.5187C>G NP_001394892.1:p.Ile1729Met missense NM_001407964.1:c.5112C>G NP_001394893.1:p.Ile1704Met missense NM_001407965.1:c.5067C>G NP_001394894.1:p.Ile1689Met missense NM_001407966.1:c.4686C>G NP_001394895.1:p.Ile1562Met missense NM_001407967.1:c.4683C>G NP_001394896.1:p.Ile1561Met missense NM_001407968.1:c.2970C>G NP_001394897.1:p.Ile990Met missense NM_001407969.1:c.2967C>G NP_001394898.1:p.Ile989Met missense NM_001407970.1:c.2331C>G NP_001394899.1:p.Ile777Met missense NM_001407971.1:c.2331C>G NP_001394900.1:p.Ile777Met missense NM_001407972.1:c.2328C>G NP_001394901.1:p.Ile776Met missense NM_001407973.1:c.2265C>G NP_001394902.1:p.Ile755Met missense NM_001407974.1:c.2265C>G NP_001394903.1:p.Ile755Met missense NM_001407975.1:c.2265C>G NP_001394904.1:p.Ile755Met missense NM_001407976.1:c.2265C>G NP_001394905.1:p.Ile755Met missense NM_001407977.1:c.2265C>G NP_001394906.1:p.Ile755Met missense NM_001407978.1:c.2265C>G NP_001394907.1:p.Ile755Met missense NM_001407979.1:c.2262C>G NP_001394908.1:p.Ile754Met missense NM_001407980.1:c.2262C>G NP_001394909.1:p.Ile754Met missense NM_001407981.1:c.2262C>G NP_001394910.1:p.Ile754Met missense NM_001407982.1:c.2262C>G NP_001394911.1:p.Ile754Met missense NM_001407983.1:c.2262C>G NP_001394912.1:p.Ile754Met missense NM_001407984.1:c.2262C>G NP_001394913.1:p.Ile754Met missense NM_001407985.1:c.2262C>G NP_001394914.1:p.Ile754Met missense NM_001407986.1:c.2262C>G NP_001394915.1:p.Ile754Met missense NM_001407990.1:c.2262C>G NP_001394919.1:p.Ile754Met missense NM_001407991.1:c.2262C>G NP_001394920.1:p.Ile754Met missense NM_001407992.1:c.2262C>G NP_001394921.1:p.Ile754Met missense NM_001407993.1:c.2262C>G NP_001394922.1:p.Ile754Met missense NM_001408392.1:c.2259C>G NP_001395321.1:p.Ile753Met missense NM_001408396.1:c.2259C>G NP_001395325.1:p.Ile753Met missense NM_001408397.1:c.2259C>G NP_001395326.1:p.Ile753Met missense NM_001408398.1:c.2259C>G NP_001395327.1:p.Ile753Met missense NM_001408399.1:c.2259C>G NP_001395328.1:p.Ile753Met missense NM_001408400.1:c.2259C>G NP_001395329.1:p.Ile753Met missense NM_001408401.1:c.2259C>G NP_001395330.1:p.Ile753Met missense NM_001408402.1:c.2259C>G NP_001395331.1:p.Ile753Met missense NM_001408403.1:c.2259C>G NP_001395332.1:p.Ile753Met missense NM_001408404.1:c.2259C>G NP_001395333.1:p.Ile753Met missense NM_001408406.1:c.2256C>G NP_001395335.1:p.Ile752Met missense NM_001408407.1:c.2256C>G NP_001395336.1:p.Ile752Met missense NM_001408408.1:c.2256C>G NP_001395337.1:p.Ile752Met missense NM_001408409.1:c.2253C>G NP_001395338.1:p.Ile751Met missense NM_001408410.1:c.2190C>G NP_001395339.1:p.Ile730Met missense NM_001408411.1:c.2187C>G NP_001395340.1:p.Ile729Met missense NM_001408412.1:c.2184C>G NP_001395341.1:p.Ile728Met missense NM_001408413.1:c.2184C>G NP_001395342.1:p.Ile728Met missense NM_001408414.1:c.2184C>G NP_001395343.1:p.Ile728Met missense NM_001408415.1:c.2184C>G NP_001395344.1:p.Ile728Met missense NM_001408416.1:c.2184C>G NP_001395345.1:p.Ile728Met missense NM_001408418.1:c.2148C>G NP_001395347.1:p.Ile716Met missense NM_001408419.1:c.2148C>G NP_001395348.1:p.Ile716Met missense NM_001408420.1:c.2148C>G NP_001395349.1:p.Ile716Met missense NM_001408421.1:c.2145C>G NP_001395350.1:p.Ile715Met missense NM_001408422.1:c.2145C>G NP_001395351.1:p.Ile715Met missense NM_001408423.1:c.2145C>G NP_001395352.1:p.Ile715Met missense NM_001408424.1:c.2145C>G NP_001395353.1:p.Ile715Met missense NM_001408425.1:c.2142C>G NP_001395354.1:p.Ile714Met missense NM_001408426.1:c.2142C>G NP_001395355.1:p.Ile714Met missense NM_001408427.1:c.2142C>G NP_001395356.1:p.Ile714Met missense NM_001408428.1:c.2142C>G NP_001395357.1:p.Ile714Met missense NM_001408429.1:c.2142C>G NP_001395358.1:p.Ile714Met missense NM_001408430.1:c.2142C>G NP_001395359.1:p.Ile714Met missense NM_001408431.1:c.2142C>G NP_001395360.1:p.Ile714Met missense NM_001408432.1:c.2139C>G NP_001395361.1:p.Ile713Met missense NM_001408433.1:c.2139C>G NP_001395362.1:p.Ile713Met missense NM_001408434.1:c.2139C>G NP_001395363.1:p.Ile713Met missense NM_001408435.1:c.2139C>G NP_001395364.1:p.Ile713Met missense NM_001408436.1:c.2139C>G NP_001395365.1:p.Ile713Met missense NM_001408437.1:c.2139C>G NP_001395366.1:p.Ile713Met missense NM_001408438.1:c.2139C>G NP_001395367.1:p.Ile713Met missense NM_001408439.1:c.2139C>G NP_001395368.1:p.Ile713Met missense NM_001408440.1:c.2139C>G NP_001395369.1:p.Ile713Met missense NM_001408441.1:c.2139C>G NP_001395370.1:p.Ile713Met missense NM_001408442.1:c.2139C>G NP_001395371.1:p.Ile713Met missense NM_001408443.1:c.2139C>G NP_001395372.1:p.Ile713Met missense NM_001408444.1:c.2139C>G NP_001395373.1:p.Ile713Met missense NM_001408445.1:c.2136C>G NP_001395374.1:p.Ile712Met missense NM_001408446.1:c.2136C>G NP_001395375.1:p.Ile712Met missense NM_001408447.1:c.2136C>G NP_001395376.1:p.Ile712Met missense NM_001408448.1:c.2136C>G NP_001395377.1:p.Ile712Met missense NM_001408450.1:c.2136C>G NP_001395379.1:p.Ile712Met missense NM_001408451.1:c.2130C>G NP_001395380.1:p.Ile710Met missense NM_001408452.1:c.2124C>G NP_001395381.1:p.Ile708Met missense NM_001408453.1:c.2124C>G NP_001395382.1:p.Ile708Met missense NM_001408454.1:c.2124C>G NP_001395383.1:p.Ile708Met missense NM_001408455.1:c.2124C>G NP_001395384.1:p.Ile708Met missense NM_001408456.1:c.2124C>G NP_001395385.1:p.Ile708Met missense NM_001408457.1:c.2124C>G NP_001395386.1:p.Ile708Met missense NM_001408458.1:c.2121C>G NP_001395387.1:p.Ile707Met missense NM_001408459.1:c.2121C>G NP_001395388.1:p.Ile707Met missense NM_001408460.1:c.2121C>G NP_001395389.1:p.Ile707Met missense NM_001408461.1:c.2121C>G NP_001395390.1:p.Ile707Met missense NM_001408462.1:c.2121C>G NP_001395391.1:p.Ile707Met missense NM_001408463.1:c.2121C>G NP_001395392.1:p.Ile707Met missense NM_001408464.1:c.2121C>G NP_001395393.1:p.Ile707Met missense NM_001408465.1:c.2121C>G NP_001395394.1:p.Ile707Met missense NM_001408466.1:c.2121C>G NP_001395395.1:p.Ile707Met missense NM_001408467.1:c.2121C>G NP_001395396.1:p.Ile707Met missense NM_001408468.1:c.2118C>G NP_001395397.1:p.Ile706Met missense NM_001408469.1:c.2118C>G NP_001395398.1:p.Ile706Met missense NM_001408470.1:c.2118C>G NP_001395399.1:p.Ile706Met missense NM_001408472.1:c.*88C>G NM_001408473.1:c.*88C>G NM_001408474.1:c.2064C>G NP_001395403.1:p.Ile688Met missense NM_001408475.1:c.2061C>G NP_001395404.1:p.Ile687Met missense NM_001408476.1:c.2061C>G NP_001395405.1:p.Ile687Met missense NM_001408478.1:c.2055C>G NP_001395407.1:p.Ile685Met missense NM_001408479.1:c.2055C>G NP_001395408.1:p.Ile685Met missense NM_001408480.1:c.2055C>G NP_001395409.1:p.Ile685Met missense NM_001408481.1:c.2052C>G NP_001395410.1:p.Ile684Met missense NM_001408482.1:c.2052C>G NP_001395411.1:p.Ile684Met missense NM_001408483.1:c.2052C>G NP_001395412.1:p.Ile684Met missense NM_001408484.1:c.2052C>G NP_001395413.1:p.Ile684Met missense NM_001408485.1:c.2052C>G NP_001395414.1:p.Ile684Met missense NM_001408489.1:c.2052C>G NP_001395418.1:p.Ile684Met missense NM_001408490.1:c.2052C>G NP_001395419.1:p.Ile684Met missense NM_001408491.1:c.2052C>G NP_001395420.1:p.Ile684Met missense NM_001408492.1:c.2049C>G NP_001395421.1:p.Ile683Met missense NM_001408493.1:c.2049C>G NP_001395422.1:p.Ile683Met missense NM_001408494.1:c.2025C>G NP_001395423.1:p.Ile675Met missense NM_001408495.1:c.2019C>G NP_001395424.1:p.Ile673Met missense NM_001408496.1:c.2001C>G NP_001395425.1:p.Ile667Met missense NM_001408497.1:c.2001C>G NP_001395426.1:p.Ile667Met missense NM_001408498.1:c.2001C>G NP_001395427.1:p.Ile667Met missense NM_001408499.1:c.2001C>G NP_001395428.1:p.Ile667Met missense NM_001408500.1:c.2001C>G NP_001395429.1:p.Ile667Met missense NM_001408501.1:c.2001C>G NP_001395430.1:p.Ile667Met missense NM_001408502.1:c.1998C>G NP_001395431.1:p.Ile666Met missense NM_001408503.1:c.1998C>G NP_001395432.1:p.Ile666Met missense NM_001408504.1:c.1998C>G NP_001395433.1:p.Ile666Met missense NM_001408505.1:c.1995C>G NP_001395434.1:p.Ile665Met missense NM_001408506.1:c.1938C>G NP_001395435.1:p.Ile646Met missense NM_001408507.1:c.1935C>G NP_001395436.1:p.Ile645Met missense NM_001408508.1:c.1926C>G NP_001395437.1:p.Ile642Met missense NM_001408509.1:c.1923C>G NP_001395438.1:p.Ile641Met missense NM_001408510.1:c.1884C>G NP_001395439.1:p.Ile628Met missense NM_001408511.1:c.1881C>G NP_001395440.1:p.Ile627Met missense NM_001408512.1:c.1761C>G NP_001395441.1:p.Ile587Met missense NM_001408513.1:c.1734C>G NP_001395442.1:p.Ile578Met missense NM_001408514.1:c.1338C>G NP_001395443.1:p.Ile446Met missense NM_007297.4:c.5433C>G NP_009228.2:p.Ile1811Met missense NM_007298.4:c.2262C>G NP_009229.2:p.Ile754Met missense NM_007299.4:c.*88C>G 3 prime UTR NM_007300.4:c.5637C>G NP_009231.2:p.Ile1879Met missense NM_007304.2:c.2262C>G NP_009235.2:p.Ile754Met missense NR_027676.2:n.5751C>G non-coding transcript variant NC_000017.11:g.43045696G>C NC_000017.10:g.41197713G>C NG_005905.2:g.172288C>G LRG_292:g.172288C>G LRG_292t1:c.5574C>G LRG_292p1:p.Ile1858Met - Protein change
- I1858M, I1811M, I1879M, I754M, I1561M, I1689M, I1731M, I1788M, I1789M, I1790M, I1817M, I1830M, I1831M, I1853M, I1855M, I1878M, I1880M, I587M, I628M, I645M, I665M, I666M, I687M, I707M, I712M, I714M, I777M, I990M, I1768M, I1786M, I1787M, I1810M, I1832M, I1838M, I1854M, I1856M, I627M, I641M, I667M, I673M, I675M, I688M, I716M, I729M, I751M, I753M, I755M, I1745M, I1770M, I1809M, I1814M, I1815M, I1839M, I1857M, I646M, I683M, I706M, I708M, I710M, I730M, I1562M, I1704M, I1729M, I1730M, I1746M, I1747M, I1769M, I1774M, I1791M, I1816M, I446M, I578M, I642M, I684M, I685M, I713M, I715M, I728M, I752M, I776M, I989M
- Other names
- -
- Canonical SPDI
- NC_000017.11:43045695:G:C
-
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), exomes 0.00000
Trans-Omics for Precision Medicine (TOPMed) 0.00001
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 |
13016 | 14818 |
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 (1) |
criteria provided, single submitter
|
Feb 20, 2017 | RCV000507156.3 | |
Uncertain significance (1) |
criteria provided, single submitter
|
Aug 9, 2022 | RCV000637606.11 | |
Uncertain significance (1) |
criteria provided, single submitter
|
Jun 13, 2023 | RCV000564494.6 | |
Uncertain significance (1) |
criteria provided, single submitter
|
Jan 17, 2023 | RCV001540362.4 |
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
(Feb 20, 2017)
|
criteria provided, single submitter
Method: clinical testing
|
not specified
Affected status: unknown
Allele origin:
germline
|
Quest Diagnostics Nichols Institute San Juan Capistrano
Accession: SCV000600428.2
First in ClinVar: Sep 30, 2017 Last updated: Jan 01, 2022 |
|
|
Uncertain significance
(Jan 17, 2023)
|
criteria provided, single submitter
Method: clinical testing
|
Not Provided
Affected status: yes
Allele origin:
germline
|
GeneDx
Accession: SCV001758239.2
First in ClinVar: Jul 24, 2021 Last updated: Feb 07, 2023 |
Comment:
Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant does not alter protein structure/function; Has not … (more)
Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; Also known as 5693C>G (less)
|
|
Uncertain significance
(Aug 09, 2022)
|
criteria provided, single submitter
Method: clinical testing
|
Hereditary breast ovarian cancer syndrome
Affected status: unknown
Allele origin:
germline
|
Invitae
Accession: SCV000759072.8
First in ClinVar: May 28, 2018 Last updated: Feb 14, 2024 |
Comment:
This variant is present in population databases (no rsID available, gnomAD 0.0009%). In summary, the available evidence is currently insufficient to determine the role of … (more)
This variant is present in population databases (no rsID available, gnomAD 0.0009%). 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: 438943). This variant has not been reported in the literature in individuals affected with BRCA1-related conditions. This sequence change replaces isoleucine, which is neutral and non-polar, with methionine, which is neutral and non-polar, at codon 1858 of the BRCA1 protein (p.Ile1858Met). (less)
|
|
Uncertain significance
(Jun 13, 2023)
|
criteria provided, single submitter
Method: clinical testing
|
Hereditary cancer-predisposing syndrome
Affected status: unknown
Allele origin:
germline
|
Ambry Genetics
Accession: SCV000661031.6
First in ClinVar: Jan 01, 2018 Last updated: May 01, 2024 |
Comment:
The p.I1858M variant (also known as c.5574C>G), located in coding exon 22 of the BRCA1 gene, results from a C to G substitution at nucleotide … (more)
The p.I1858M variant (also known as c.5574C>G), located in coding exon 22 of the BRCA1 gene, results from a C to G substitution at nucleotide position 5574. The isoleucine at codon 1858 is replaced by methionine, 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)
|
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
HelpThere are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar. |
Text-mined citations for rs876659941 ...
HelpRecord last updated Jul 15, 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.