ACMG codes applied following ENIGMA VCEP rules: PM2_SUP
ClinVar Genomic variation as it relates to human health
NM_007294.4(BRCA1):c.4445A>G (p.Asp1482Gly)
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.
(4)
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
4
criteria provided, multiple submitters, no conflicts
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Variant Details
- Identifiers
-
NM_007294.4(BRCA1):c.4445A>G (p.Asp1482Gly)
Variation ID: 808278 Accession: VCV000808278.25
- Type and length
-
single nucleotide variant, 1 bp
- Location
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Cytogenetic: 17q21.31 17: 43076527 (GRCh38) [ NCBI UCSC ] 17: 41228544 (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 Feb 3, 2020 Jun 17, 2024 Feb 9, 2024 - HGVS
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... more HGVS ... less HGVSNucleotide Protein Molecular
consequenceNM_007294.4:c.4445A>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NP_009225.1:p.Asp1482Gly missense NM_001407571.1:c.4232A>G NP_001394500.1:p.Asp1411Gly missense NM_001407581.1:c.4511A>G NP_001394510.1:p.Asp1504Gly missense NM_001407582.1:c.4511A>G NP_001394511.1:p.Asp1504Gly missense NM_001407583.1:c.4508A>G NP_001394512.1:p.Asp1503Gly missense NM_001407585.1:c.4508A>G NP_001394514.1:p.Asp1503Gly missense NM_001407587.1:c.4508A>G NP_001394516.1:p.Asp1503Gly missense NM_001407590.1:c.4505A>G NP_001394519.1:p.Asp1502Gly missense NM_001407591.1:c.4505A>G NP_001394520.1:p.Asp1502Gly missense NM_001407593.1:c.4445A>G NP_001394522.1:p.Asp1482Gly missense NM_001407594.1:c.4445A>G NP_001394523.1:p.Asp1482Gly missense NM_001407596.1:c.4445A>G NP_001394525.1:p.Asp1482Gly missense NM_001407597.1:c.4445A>G NP_001394526.1:p.Asp1482Gly missense NM_001407598.1:c.4445A>G NP_001394527.1:p.Asp1482Gly missense NM_001407602.1:c.4445A>G NP_001394531.1:p.Asp1482Gly missense NM_001407603.1:c.4445A>G NP_001394532.1:p.Asp1482Gly missense NM_001407605.1:c.4445A>G NP_001394534.1:p.Asp1482Gly missense NM_001407610.1:c.4442A>G NP_001394539.1:p.Asp1481Gly missense NM_001407611.1:c.4442A>G NP_001394540.1:p.Asp1481Gly missense NM_001407612.1:c.4442A>G NP_001394541.1:p.Asp1481Gly missense NM_001407613.1:c.4442A>G NP_001394542.1:p.Asp1481Gly missense NM_001407614.1:c.4442A>G NP_001394543.1:p.Asp1481Gly missense NM_001407615.1:c.4442A>G NP_001394544.1:p.Asp1481Gly missense NM_001407616.1:c.4442A>G NP_001394545.1:p.Asp1481Gly missense NM_001407617.1:c.4442A>G NP_001394546.1:p.Asp1481Gly missense NM_001407618.1:c.4442A>G NP_001394547.1:p.Asp1481Gly missense NM_001407619.1:c.4442A>G NP_001394548.1:p.Asp1481Gly missense NM_001407620.1:c.4442A>G NP_001394549.1:p.Asp1481Gly missense NM_001407621.1:c.4442A>G NP_001394550.1:p.Asp1481Gly missense NM_001407622.1:c.4442A>G NP_001394551.1:p.Asp1481Gly missense NM_001407623.1:c.4442A>G NP_001394552.1:p.Asp1481Gly missense NM_001407624.1:c.4442A>G NP_001394553.1:p.Asp1481Gly missense NM_001407625.1:c.4442A>G NP_001394554.1:p.Asp1481Gly missense NM_001407626.1:c.4442A>G NP_001394555.1:p.Asp1481Gly missense NM_001407627.1:c.4439A>G NP_001394556.1:p.Asp1480Gly missense NM_001407628.1:c.4439A>G NP_001394557.1:p.Asp1480Gly missense NM_001407629.1:c.4439A>G NP_001394558.1:p.Asp1480Gly missense NM_001407630.1:c.4439A>G NP_001394559.1:p.Asp1480Gly missense NM_001407631.1:c.4439A>G NP_001394560.1:p.Asp1480Gly missense NM_001407632.1:c.4439A>G NP_001394561.1:p.Asp1480Gly missense NM_001407633.1:c.4439A>G NP_001394562.1:p.Asp1480Gly missense NM_001407634.1:c.4439A>G NP_001394563.1:p.Asp1480Gly missense NM_001407635.1:c.4439A>G NP_001394564.1:p.Asp1480Gly missense NM_001407636.1:c.4439A>G NP_001394565.1:p.Asp1480Gly missense NM_001407637.1:c.4439A>G NP_001394566.1:p.Asp1480Gly missense NM_001407638.1:c.4439A>G NP_001394567.1:p.Asp1480Gly missense NM_001407639.1:c.4439A>G NP_001394568.1:p.Asp1480Gly missense NM_001407640.1:c.4439A>G NP_001394569.1:p.Asp1480Gly missense NM_001407641.1:c.4439A>G NP_001394570.1:p.Asp1480Gly missense NM_001407642.1:c.4439A>G NP_001394571.1:p.Asp1480Gly missense NM_001407644.1:c.4436A>G NP_001394573.1:p.Asp1479Gly missense NM_001407645.1:c.4436A>G NP_001394574.1:p.Asp1479Gly missense NM_001407646.1:c.4433A>G NP_001394575.1:p.Asp1478Gly missense NM_001407647.1:c.4430A>G NP_001394576.1:p.Asp1477Gly missense NM_001407648.1:c.4388A>G NP_001394577.1:p.Asp1463Gly missense NM_001407649.1:c.4385A>G NP_001394578.1:p.Asp1462Gly missense NM_001407652.1:c.4445A>G NP_001394581.1:p.Asp1482Gly missense NM_001407653.1:c.4367A>G NP_001394582.1:p.Asp1456Gly missense NM_001407654.1:c.4367A>G NP_001394583.1:p.Asp1456Gly missense NM_001407655.1:c.4367A>G NP_001394584.1:p.Asp1456Gly missense NM_001407656.1:c.4364A>G NP_001394585.1:p.Asp1455Gly missense NM_001407657.1:c.4364A>G NP_001394586.1:p.Asp1455Gly missense NM_001407658.1:c.4364A>G NP_001394587.1:p.Asp1455Gly missense NM_001407659.1:c.4361A>G NP_001394588.1:p.Asp1454Gly missense NM_001407660.1:c.4361A>G NP_001394589.1:p.Asp1454Gly missense NM_001407661.1:c.4361A>G NP_001394590.1:p.Asp1454Gly missense NM_001407662.1:c.4361A>G NP_001394591.1:p.Asp1454Gly missense NM_001407663.1:c.4361A>G NP_001394592.1:p.Asp1454Gly missense NM_001407664.1:c.4322A>G NP_001394593.1:p.Asp1441Gly missense NM_001407665.1:c.4322A>G NP_001394594.1:p.Asp1441Gly missense NM_001407666.1:c.4322A>G NP_001394595.1:p.Asp1441Gly missense NM_001407667.1:c.4322A>G NP_001394596.1:p.Asp1441Gly missense NM_001407668.1:c.4322A>G NP_001394597.1:p.Asp1441Gly missense NM_001407669.1:c.4322A>G NP_001394598.1:p.Asp1441Gly missense NM_001407670.1:c.4319A>G NP_001394599.1:p.Asp1440Gly missense NM_001407671.1:c.4319A>G NP_001394600.1:p.Asp1440Gly missense NM_001407672.1:c.4319A>G NP_001394601.1:p.Asp1440Gly missense NM_001407673.1:c.4319A>G NP_001394602.1:p.Asp1440Gly missense NM_001407674.1:c.4319A>G NP_001394603.1:p.Asp1440Gly missense NM_001407675.1:c.4319A>G NP_001394604.1:p.Asp1440Gly missense NM_001407676.1:c.4319A>G NP_001394605.1:p.Asp1440Gly missense NM_001407677.1:c.4319A>G NP_001394606.1:p.Asp1440Gly missense NM_001407678.1:c.4319A>G NP_001394607.1:p.Asp1440Gly missense NM_001407679.1:c.4319A>G NP_001394608.1:p.Asp1440Gly missense NM_001407680.1:c.4319A>G NP_001394609.1:p.Asp1440Gly missense NM_001407681.1:c.4316A>G NP_001394610.1:p.Asp1439Gly missense NM_001407682.1:c.4316A>G NP_001394611.1:p.Asp1439Gly missense NM_001407683.1:c.4316A>G NP_001394612.1:p.Asp1439Gly missense NM_001407684.1:c.4445A>G NP_001394613.1:p.Asp1482Gly missense NM_001407685.1:c.4316A>G NP_001394614.1:p.Asp1439Gly missense NM_001407686.1:c.4316A>G NP_001394615.1:p.Asp1439Gly missense NM_001407687.1:c.4316A>G NP_001394616.1:p.Asp1439Gly missense NM_001407688.1:c.4316A>G NP_001394617.1:p.Asp1439Gly missense NM_001407689.1:c.4316A>G NP_001394618.1:p.Asp1439Gly missense NM_001407690.1:c.4313A>G NP_001394619.1:p.Asp1438Gly missense NM_001407691.1:c.4313A>G NP_001394620.1:p.Asp1438Gly missense NM_001407692.1:c.4304A>G NP_001394621.1:p.Asp1435Gly missense NM_001407694.1:c.4304A>G NP_001394623.1:p.Asp1435Gly missense NM_001407695.1:c.4304A>G NP_001394624.1:p.Asp1435Gly missense NM_001407696.1:c.4304A>G NP_001394625.1:p.Asp1435Gly missense NM_001407697.1:c.4304A>G NP_001394626.1:p.Asp1435Gly missense NM_001407698.1:c.4304A>G NP_001394627.1:p.Asp1435Gly missense NM_001407724.1:c.4304A>G NP_001394653.1:p.Asp1435Gly missense NM_001407725.1:c.4304A>G NP_001394654.1:p.Asp1435Gly missense NM_001407726.1:c.4304A>G NP_001394655.1:p.Asp1435Gly missense NM_001407727.1:c.4304A>G NP_001394656.1:p.Asp1435Gly missense NM_001407728.1:c.4304A>G NP_001394657.1:p.Asp1435Gly missense NM_001407729.1:c.4304A>G NP_001394658.1:p.Asp1435Gly missense NM_001407730.1:c.4304A>G NP_001394659.1:p.Asp1435Gly missense NM_001407731.1:c.4304A>G NP_001394660.1:p.Asp1435Gly missense NM_001407732.1:c.4301A>G NP_001394661.1:p.Asp1434Gly missense NM_001407733.1:c.4301A>G NP_001394662.1:p.Asp1434Gly missense NM_001407734.1:c.4301A>G NP_001394663.1:p.Asp1434Gly missense NM_001407735.1:c.4301A>G NP_001394664.1:p.Asp1434Gly missense NM_001407736.1:c.4301A>G NP_001394665.1:p.Asp1434Gly missense NM_001407737.1:c.4301A>G NP_001394666.1:p.Asp1434Gly missense NM_001407738.1:c.4301A>G NP_001394667.1:p.Asp1434Gly missense NM_001407739.1:c.4301A>G NP_001394668.1:p.Asp1434Gly missense NM_001407740.1:c.4301A>G NP_001394669.1:p.Asp1434Gly missense NM_001407741.1:c.4301A>G NP_001394670.1:p.Asp1434Gly missense NM_001407742.1:c.4301A>G NP_001394671.1:p.Asp1434Gly missense NM_001407743.1:c.4301A>G NP_001394672.1:p.Asp1434Gly missense NM_001407744.1:c.4301A>G NP_001394673.1:p.Asp1434Gly missense NM_001407745.1:c.4301A>G NP_001394674.1:p.Asp1434Gly missense NM_001407746.1:c.4301A>G NP_001394675.1:p.Asp1434Gly missense NM_001407747.1:c.4301A>G NP_001394676.1:p.Asp1434Gly missense NM_001407748.1:c.4301A>G NP_001394677.1:p.Asp1434Gly missense NM_001407749.1:c.4301A>G NP_001394678.1:p.Asp1434Gly missense NM_001407750.1:c.4301A>G NP_001394679.1:p.Asp1434Gly missense NM_001407751.1:c.4301A>G NP_001394680.1:p.Asp1434Gly missense NM_001407752.1:c.4301A>G NP_001394681.1:p.Asp1434Gly missense NM_001407838.1:c.4298A>G NP_001394767.1:p.Asp1433Gly missense NM_001407839.1:c.4298A>G NP_001394768.1:p.Asp1433Gly missense NM_001407841.1:c.4298A>G NP_001394770.1:p.Asp1433Gly missense NM_001407842.1:c.4298A>G NP_001394771.1:p.Asp1433Gly missense NM_001407843.1:c.4298A>G NP_001394772.1:p.Asp1433Gly missense NM_001407844.1:c.4298A>G NP_001394773.1:p.Asp1433Gly missense NM_001407845.1:c.4298A>G NP_001394774.1:p.Asp1433Gly missense NM_001407846.1:c.4298A>G NP_001394775.1:p.Asp1433Gly missense NM_001407847.1:c.4298A>G NP_001394776.1:p.Asp1433Gly missense NM_001407848.1:c.4298A>G NP_001394777.1:p.Asp1433Gly missense NM_001407849.1:c.4298A>G NP_001394778.1:p.Asp1433Gly missense NM_001407850.1:c.4298A>G NP_001394779.1:p.Asp1433Gly missense NM_001407851.1:c.4298A>G NP_001394780.1:p.Asp1433Gly missense NM_001407852.1:c.4298A>G NP_001394781.1:p.Asp1433Gly missense NM_001407853.1:c.4298A>G NP_001394782.1:p.Asp1433Gly missense NM_001407854.1:c.4445A>G NP_001394783.1:p.Asp1482Gly missense NM_001407858.1:c.4442A>G NP_001394787.1:p.Asp1481Gly missense NM_001407859.1:c.4442A>G NP_001394788.1:p.Asp1481Gly missense NM_001407860.1:c.4442A>G NP_001394789.1:p.Asp1481Gly missense NM_001407861.1:c.4439A>G NP_001394790.1:p.Asp1480Gly missense NM_001407862.1:c.4244A>G NP_001394791.1:p.Asp1415Gly missense NM_001407863.1:c.4319A>G NP_001394792.1:p.Asp1440Gly missense NM_001407874.1:c.4238A>G NP_001394803.1:p.Asp1413Gly missense NM_001407875.1:c.4238A>G NP_001394804.1:p.Asp1413Gly missense NM_001407879.1:c.4235A>G NP_001394808.1:p.Asp1412Gly missense NM_001407881.1:c.4235A>G NP_001394810.1:p.Asp1412Gly missense NM_001407882.1:c.4235A>G NP_001394811.1:p.Asp1412Gly missense NM_001407884.1:c.4235A>G NP_001394813.1:p.Asp1412Gly missense NM_001407885.1:c.4235A>G NP_001394814.1:p.Asp1412Gly missense NM_001407886.1:c.4235A>G NP_001394815.1:p.Asp1412Gly missense NM_001407887.1:c.4235A>G NP_001394816.1:p.Asp1412Gly missense NM_001407889.1:c.4235A>G NP_001394818.1:p.Asp1412Gly missense NM_001407894.1:c.4232A>G NP_001394823.1:p.Asp1411Gly missense NM_001407895.1:c.4232A>G NP_001394824.1:p.Asp1411Gly missense NM_001407896.1:c.4232A>G NP_001394825.1:p.Asp1411Gly missense NM_001407897.1:c.4232A>G NP_001394826.1:p.Asp1411Gly missense NM_001407898.1:c.4232A>G NP_001394827.1:p.Asp1411Gly missense NM_001407899.1:c.4232A>G NP_001394828.1:p.Asp1411Gly missense NM_001407900.1:c.4232A>G NP_001394829.1:p.Asp1411Gly missense NM_001407902.1:c.4232A>G NP_001394831.1:p.Asp1411Gly missense NM_001407904.1:c.4232A>G NP_001394833.1:p.Asp1411Gly missense NM_001407906.1:c.4232A>G NP_001394835.1:p.Asp1411Gly missense NM_001407907.1:c.4232A>G NP_001394836.1:p.Asp1411Gly missense NM_001407908.1:c.4232A>G NP_001394837.1:p.Asp1411Gly missense NM_001407909.1:c.4232A>G NP_001394838.1:p.Asp1411Gly missense NM_001407910.1:c.4232A>G NP_001394839.1:p.Asp1411Gly missense NM_001407915.1:c.4229A>G NP_001394844.1:p.Asp1410Gly missense NM_001407916.1:c.4229A>G NP_001394845.1:p.Asp1410Gly missense NM_001407917.1:c.4229A>G NP_001394846.1:p.Asp1410Gly missense NM_001407918.1:c.4229A>G NP_001394847.1:p.Asp1410Gly missense NM_001407919.1:c.4322A>G NP_001394848.1:p.Asp1441Gly missense NM_001407920.1:c.4181A>G NP_001394849.1:p.Asp1394Gly missense NM_001407921.1:c.4181A>G NP_001394850.1:p.Asp1394Gly missense NM_001407922.1:c.4181A>G NP_001394851.1:p.Asp1394Gly missense NM_001407923.1:c.4181A>G NP_001394852.1:p.Asp1394Gly missense NM_001407924.1:c.4181A>G NP_001394853.1:p.Asp1394Gly missense NM_001407925.1:c.4181A>G NP_001394854.1:p.Asp1394Gly missense NM_001407926.1:c.4181A>G NP_001394855.1:p.Asp1394Gly missense NM_001407927.1:c.4178A>G NP_001394856.1:p.Asp1393Gly missense NM_001407928.1:c.4178A>G NP_001394857.1:p.Asp1393Gly missense NM_001407929.1:c.4178A>G NP_001394858.1:p.Asp1393Gly missense NM_001407930.1:c.4178A>G NP_001394859.1:p.Asp1393Gly missense NM_001407931.1:c.4178A>G NP_001394860.1:p.Asp1393Gly missense NM_001407932.1:c.4178A>G NP_001394861.1:p.Asp1393Gly missense NM_001407933.1:c.4178A>G NP_001394862.1:p.Asp1393Gly missense NM_001407934.1:c.4175A>G NP_001394863.1:p.Asp1392Gly missense NM_001407935.1:c.4175A>G NP_001394864.1:p.Asp1392Gly missense NM_001407936.1:c.4175A>G NP_001394865.1:p.Asp1392Gly missense NM_001407937.1:c.4322A>G NP_001394866.1:p.Asp1441Gly missense NM_001407938.1:c.4322A>G NP_001394867.1:p.Asp1441Gly missense NM_001407939.1:c.4319A>G NP_001394868.1:p.Asp1440Gly missense NM_001407940.1:c.4319A>G NP_001394869.1:p.Asp1440Gly missense NM_001407941.1:c.4316A>G NP_001394870.1:p.Asp1439Gly missense NM_001407942.1:c.4304A>G NP_001394871.1:p.Asp1435Gly missense NM_001407943.1:c.4301A>G NP_001394872.1:p.Asp1434Gly missense NM_001407944.1:c.4301A>G NP_001394873.1:p.Asp1434Gly missense NM_001407945.1:c.4301A>G NP_001394874.1:p.Asp1434Gly missense NM_001407946.1:c.4112A>G NP_001394875.1:p.Asp1371Gly missense NM_001407947.1:c.4112A>G NP_001394876.1:p.Asp1371Gly missense NM_001407948.1:c.4112A>G NP_001394877.1:p.Asp1371Gly missense NM_001407949.1:c.4112A>G NP_001394878.1:p.Asp1371Gly missense NM_001407950.1:c.4109A>G NP_001394879.1:p.Asp1370Gly missense NM_001407951.1:c.4109A>G NP_001394880.1:p.Asp1370Gly missense NM_001407952.1:c.4109A>G NP_001394881.1:p.Asp1370Gly missense NM_001407953.1:c.4109A>G NP_001394882.1:p.Asp1370Gly missense NM_001407954.1:c.4109A>G NP_001394883.1:p.Asp1370Gly missense NM_001407955.1:c.4109A>G NP_001394884.1:p.Asp1370Gly missense NM_001407956.1:c.4106A>G NP_001394885.1:p.Asp1369Gly missense NM_001407957.1:c.4106A>G NP_001394886.1:p.Asp1369Gly missense NM_001407958.1:c.4106A>G NP_001394887.1:p.Asp1369Gly missense NM_001407959.1:c.4064A>G NP_001394888.1:p.Asp1355Gly missense NM_001407960.1:c.4061A>G NP_001394889.1:p.Asp1354Gly missense NM_001407962.1:c.4061A>G NP_001394891.1:p.Asp1354Gly missense NM_001407963.1:c.4058A>G NP_001394892.1:p.Asp1353Gly missense NM_001407965.1:c.3938A>G NP_001394894.1:p.Asp1313Gly missense NM_001407966.1:c.3557A>G NP_001394895.1:p.Asp1186Gly missense NM_001407967.1:c.3554A>G NP_001394896.1:p.Asp1185Gly missense NM_001407968.1:c.1841A>G NP_001394897.1:p.Asp614Gly missense NM_001407969.1:c.1838A>G NP_001394898.1:p.Asp613Gly missense NM_001407970.1:c.1202A>G NP_001394899.1:p.Asp401Gly missense NM_001407971.1:c.1202A>G NP_001394900.1:p.Asp401Gly missense NM_001407972.1:c.1199A>G NP_001394901.1:p.Asp400Gly missense NM_001407973.1:c.1136A>G NP_001394902.1:p.Asp379Gly missense NM_001407974.1:c.1136A>G NP_001394903.1:p.Asp379Gly missense NM_001407975.1:c.1136A>G NP_001394904.1:p.Asp379Gly missense NM_001407976.1:c.1136A>G NP_001394905.1:p.Asp379Gly missense NM_001407977.1:c.1136A>G NP_001394906.1:p.Asp379Gly missense NM_001407978.1:c.1136A>G NP_001394907.1:p.Asp379Gly missense NM_001407979.1:c.1133A>G NP_001394908.1:p.Asp378Gly missense NM_001407980.1:c.1133A>G NP_001394909.1:p.Asp378Gly missense NM_001407981.1:c.1133A>G NP_001394910.1:p.Asp378Gly missense NM_001407982.1:c.1133A>G NP_001394911.1:p.Asp378Gly missense NM_001407983.1:c.1133A>G NP_001394912.1:p.Asp378Gly missense NM_001407984.1:c.1133A>G NP_001394913.1:p.Asp378Gly missense NM_001407985.1:c.1133A>G NP_001394914.1:p.Asp378Gly missense NM_001407986.1:c.1133A>G NP_001394915.1:p.Asp378Gly missense NM_001407990.1:c.1133A>G NP_001394919.1:p.Asp378Gly missense NM_001407991.1:c.1133A>G NP_001394920.1:p.Asp378Gly missense NM_001407992.1:c.1133A>G NP_001394921.1:p.Asp378Gly missense NM_001407993.1:c.1133A>G NP_001394922.1:p.Asp378Gly missense NM_001408392.1:c.1130A>G NP_001395321.1:p.Asp377Gly missense NM_001408396.1:c.1130A>G NP_001395325.1:p.Asp377Gly missense NM_001408397.1:c.1130A>G NP_001395326.1:p.Asp377Gly missense NM_001408398.1:c.1130A>G NP_001395327.1:p.Asp377Gly missense NM_001408399.1:c.1130A>G NP_001395328.1:p.Asp377Gly missense NM_001408400.1:c.1130A>G NP_001395329.1:p.Asp377Gly missense NM_001408401.1:c.1130A>G NP_001395330.1:p.Asp377Gly missense NM_001408402.1:c.1130A>G NP_001395331.1:p.Asp377Gly missense NM_001408403.1:c.1130A>G NP_001395332.1:p.Asp377Gly missense NM_001408404.1:c.1130A>G NP_001395333.1:p.Asp377Gly missense NM_001408406.1:c.1127A>G NP_001395335.1:p.Asp376Gly missense NM_001408407.1:c.1127A>G NP_001395336.1:p.Asp376Gly missense NM_001408408.1:c.1127A>G NP_001395337.1:p.Asp376Gly missense NM_001408409.1:c.1124A>G NP_001395338.1:p.Asp375Gly missense NM_001408410.1:c.1061A>G NP_001395339.1:p.Asp354Gly missense NM_001408411.1:c.1058A>G NP_001395340.1:p.Asp353Gly missense NM_001408412.1:c.1055A>G NP_001395341.1:p.Asp352Gly missense NM_001408413.1:c.1055A>G NP_001395342.1:p.Asp352Gly missense NM_001408414.1:c.1055A>G NP_001395343.1:p.Asp352Gly missense NM_001408415.1:c.1055A>G NP_001395344.1:p.Asp352Gly missense NM_001408416.1:c.1055A>G NP_001395345.1:p.Asp352Gly missense NM_001408418.1:c.1019A>G NP_001395347.1:p.Asp340Gly missense NM_001408419.1:c.1019A>G NP_001395348.1:p.Asp340Gly missense NM_001408420.1:c.1019A>G NP_001395349.1:p.Asp340Gly missense NM_001408421.1:c.1016A>G NP_001395350.1:p.Asp339Gly missense NM_001408422.1:c.1016A>G NP_001395351.1:p.Asp339Gly missense NM_001408423.1:c.1016A>G NP_001395352.1:p.Asp339Gly missense NM_001408424.1:c.1016A>G NP_001395353.1:p.Asp339Gly missense NM_001408425.1:c.1013A>G NP_001395354.1:p.Asp338Gly missense NM_001408426.1:c.1013A>G NP_001395355.1:p.Asp338Gly missense NM_001408427.1:c.1013A>G NP_001395356.1:p.Asp338Gly missense NM_001408428.1:c.1013A>G NP_001395357.1:p.Asp338Gly missense NM_001408429.1:c.1013A>G NP_001395358.1:p.Asp338Gly missense NM_001408430.1:c.1013A>G NP_001395359.1:p.Asp338Gly missense NM_001408431.1:c.1013A>G NP_001395360.1:p.Asp338Gly missense NM_001408432.1:c.1010A>G NP_001395361.1:p.Asp337Gly missense NM_001408433.1:c.1010A>G NP_001395362.1:p.Asp337Gly missense NM_001408434.1:c.1010A>G NP_001395363.1:p.Asp337Gly missense NM_001408435.1:c.1010A>G NP_001395364.1:p.Asp337Gly missense NM_001408436.1:c.1010A>G NP_001395365.1:p.Asp337Gly missense NM_001408437.1:c.1010A>G NP_001395366.1:p.Asp337Gly missense NM_001408438.1:c.1010A>G NP_001395367.1:p.Asp337Gly missense NM_001408439.1:c.1010A>G NP_001395368.1:p.Asp337Gly missense NM_001408440.1:c.1010A>G NP_001395369.1:p.Asp337Gly missense NM_001408441.1:c.1010A>G NP_001395370.1:p.Asp337Gly missense NM_001408442.1:c.1010A>G NP_001395371.1:p.Asp337Gly missense NM_001408443.1:c.1010A>G NP_001395372.1:p.Asp337Gly missense NM_001408444.1:c.1010A>G NP_001395373.1:p.Asp337Gly missense NM_001408445.1:c.1007A>G NP_001395374.1:p.Asp336Gly missense NM_001408446.1:c.1007A>G NP_001395375.1:p.Asp336Gly missense NM_001408447.1:c.1007A>G NP_001395376.1:p.Asp336Gly missense NM_001408448.1:c.1007A>G NP_001395377.1:p.Asp336Gly missense NM_001408450.1:c.1007A>G NP_001395379.1:p.Asp336Gly missense NM_001408451.1:c.1001A>G NP_001395380.1:p.Asp334Gly missense NM_001408452.1:c.995A>G NP_001395381.1:p.Asp332Gly missense NM_001408453.1:c.995A>G NP_001395382.1:p.Asp332Gly missense NM_001408454.1:c.995A>G NP_001395383.1:p.Asp332Gly missense NM_001408455.1:c.995A>G NP_001395384.1:p.Asp332Gly missense NM_001408456.1:c.995A>G NP_001395385.1:p.Asp332Gly missense NM_001408457.1:c.995A>G NP_001395386.1:p.Asp332Gly missense NM_001408458.1:c.992A>G NP_001395387.1:p.Asp331Gly missense NM_001408459.1:c.992A>G NP_001395388.1:p.Asp331Gly missense NM_001408460.1:c.992A>G NP_001395389.1:p.Asp331Gly missense NM_001408461.1:c.992A>G NP_001395390.1:p.Asp331Gly missense NM_001408462.1:c.992A>G NP_001395391.1:p.Asp331Gly missense NM_001408463.1:c.992A>G NP_001395392.1:p.Asp331Gly missense NM_001408464.1:c.992A>G NP_001395393.1:p.Asp331Gly missense NM_001408465.1:c.992A>G NP_001395394.1:p.Asp331Gly missense NM_001408466.1:c.992A>G NP_001395395.1:p.Asp331Gly missense NM_001408467.1:c.992A>G NP_001395396.1:p.Asp331Gly missense NM_001408468.1:c.989A>G NP_001395397.1:p.Asp330Gly missense NM_001408469.1:c.989A>G NP_001395398.1:p.Asp330Gly missense NM_001408470.1:c.989A>G NP_001395399.1:p.Asp330Gly missense NM_001408472.1:c.1133A>G NP_001395401.1:p.Asp378Gly missense NM_001408473.1:c.1130A>G NP_001395402.1:p.Asp377Gly missense NM_001408474.1:c.935A>G NP_001395403.1:p.Asp312Gly missense NM_001408475.1:c.932A>G NP_001395404.1:p.Asp311Gly missense NM_001408476.1:c.932A>G NP_001395405.1:p.Asp311Gly missense NM_001408478.1:c.926A>G NP_001395407.1:p.Asp309Gly missense NM_001408479.1:c.926A>G NP_001395408.1:p.Asp309Gly missense NM_001408480.1:c.926A>G NP_001395409.1:p.Asp309Gly missense NM_001408481.1:c.923A>G NP_001395410.1:p.Asp308Gly missense NM_001408482.1:c.923A>G NP_001395411.1:p.Asp308Gly missense NM_001408483.1:c.923A>G NP_001395412.1:p.Asp308Gly missense NM_001408484.1:c.923A>G NP_001395413.1:p.Asp308Gly missense NM_001408485.1:c.923A>G NP_001395414.1:p.Asp308Gly missense NM_001408489.1:c.923A>G NP_001395418.1:p.Asp308Gly missense NM_001408490.1:c.923A>G NP_001395419.1:p.Asp308Gly missense NM_001408491.1:c.923A>G NP_001395420.1:p.Asp308Gly missense NM_001408492.1:c.920A>G NP_001395421.1:p.Asp307Gly missense NM_001408493.1:c.920A>G NP_001395422.1:p.Asp307Gly missense NM_001408494.1:c.896A>G NP_001395423.1:p.Asp299Gly missense NM_001408495.1:c.890A>G NP_001395424.1:p.Asp297Gly missense NM_001408496.1:c.872A>G NP_001395425.1:p.Asp291Gly missense NM_001408497.1:c.872A>G NP_001395426.1:p.Asp291Gly missense NM_001408498.1:c.872A>G NP_001395427.1:p.Asp291Gly missense NM_001408499.1:c.872A>G NP_001395428.1:p.Asp291Gly missense NM_001408500.1:c.872A>G NP_001395429.1:p.Asp291Gly missense NM_001408501.1:c.872A>G NP_001395430.1:p.Asp291Gly missense NM_001408502.1:c.869A>G NP_001395431.1:p.Asp290Gly missense NM_001408503.1:c.869A>G NP_001395432.1:p.Asp290Gly missense NM_001408504.1:c.869A>G NP_001395433.1:p.Asp290Gly missense NM_001408505.1:c.866A>G NP_001395434.1:p.Asp289Gly missense NM_001408506.1:c.809A>G NP_001395435.1:p.Asp270Gly missense NM_001408507.1:c.806A>G NP_001395436.1:p.Asp269Gly missense NM_001408508.1:c.797A>G NP_001395437.1:p.Asp266Gly missense NM_001408509.1:c.794A>G NP_001395438.1:p.Asp265Gly missense NM_001408510.1:c.755A>G NP_001395439.1:p.Asp252Gly missense NM_001408511.1:c.752A>G NP_001395440.1:p.Asp251Gly missense NM_001408512.1:c.632A>G NP_001395441.1:p.Asp211Gly missense NM_007297.4:c.4304A>G NP_009228.2:p.Asp1435Gly missense NM_007298.4:c.1133A>G NP_009229.2:p.Asp378Gly missense NM_007299.4:c.1133A>G NP_009230.2:p.Asp378Gly missense NM_007300.4:c.4508A>G NP_009231.2:p.Asp1503Gly missense NM_007304.2:c.1133A>G NP_009235.2:p.Asp378Gly missense NR_027676.2:n.4622A>G non-coding transcript variant NC_000017.11:g.43076527T>C NC_000017.10:g.41228544T>C NG_005905.2:g.141457A>G LRG_292:g.141457A>G LRG_292t1:c.4445A>G LRG_292p1:p.Asp1482Gly - Protein change
- D1482G, D1503G, D378G, D1435G, D312G, D332G, D336G, D353G, D354G, D376G, D377G, D1411G, D1433G, D1438G, D1439G, D1441G, D1462G, D1479G, D251G, D265G, D270G, D289G, D297G, D307G, D308G, D1186G, D1313G, D1371G, D1410G, D1412G, D1434G, D1440G, D1463G, D1477G, D1480G, D1504G, D211G, D266G, D269G, D311G, D331G, D334G, D340G, D375G, D401G, D613G, D614G, D1185G, D1354G, D1392G, D1393G, D1394G, D1415G, D1454G, D252G, D290G, D299G, D330G, D352G, D400G, D1353G, D1355G, D1369G, D1370G, D1413G, D1455G, D1456G, D1478G, D1481G, D1502G, D291G, D309G, D337G, D338G, D339G, D379G
- Other names
- -
- Canonical SPDI
- NC_000017.11:43076526:T: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.
- -
- 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 |
13041 | 14847 | |
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
|
Jun 6, 2022 | RCV001022494.11 | |
| Uncertain significance (1) |
criteria provided, single submitter
|
Jul 19, 2021 | RCV001309906.15 | |
| Uncertain significance (1) |
criteria provided, single submitter
|
Feb 9, 2024 | RCV003607365.1 | |
| Uncertain significance (1) |
criteria provided, single submitter
|
Dec 17, 2023 | RCV004569840.1 |
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. |
|
|---|---|---|---|---|---|
|
Uncertain significance
(Feb 09, 2024)
|
criteria provided, single submitter
Method: clinical testing
|
Familial cancer of breast
Affected status: yes
Allele origin:
germline
|
MGZ Medical Genetics Center
Accession: SCV004543874.1
First in ClinVar: Feb 20, 2024 Last updated: Feb 20, 2024 |
Comment:
ACMG codes applied following ENIGMA VCEP rules: PM2_SUP
|
|
|
Uncertain significance
(Jul 19, 2021)
|
criteria provided, single submitter
Method: clinical testing
|
Hereditary breast ovarian cancer syndrome
Affected status: unknown
Allele origin:
germline
|
Labcorp Genetics (formerly Invitae), Labcorp
Accession: SCV001499420.4
First in ClinVar: Mar 07, 2021 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. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The glycine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has been observed in individual(s) with clinical features of hereditary breast and ovarian cancer syndrome (PMID: 21120943). ClinVar contains an entry for this variant (Variation ID: 808278). This variant is not present in population databases (ExAC no frequency). This sequence change replaces aspartic acid with glycine at codon 1482 of the BRCA1 protein (p.Asp1482Gly). The aspartic acid residue is moderately conserved and there is a moderate physicochemical difference between aspartic acid and glycine. (less)
|
|
|
Uncertain significance
(Jun 06, 2022)
|
criteria provided, single submitter
Method: clinical testing
|
Hereditary cancer-predisposing syndrome
Affected status: unknown
Allele origin:
germline
|
Ambry Genetics
Accession: SCV001184241.4
First in ClinVar: Mar 16, 2020 Last updated: May 01, 2024 |
Comment:
The p.D1482G variant (also known as c.4445A>G), located in coding exon 12 of the BRCA1 gene, results from an A to G substitution at nucleotide … (more)
The p.D1482G variant (also known as c.4445A>G), located in coding exon 12 of the BRCA1 gene, results from an A to G substitution at nucleotide position 4445. The aspartic acid at codon 1482 is replaced by glycine, an amino acid with similar properties. In one study, this variant was observed in 1/1525 unrelated patients who had BRCA1/2 genetic testing due to a personal and/or family history suspicious for Hereditary Breast and/or Ovarian Cancer (Caux-Moncoutier V et al. Hum. Mutat., 2011 Mar;32:325-34). This amino acid position is not well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. (less)
|
|
|
Uncertain significance
(Dec 17, 2023)
|
criteria provided, single submitter
Method: clinical testing
|
Breast-ovarian cancer, familial, susceptibility to, 1
Affected status: unknown
Allele origin:
unknown
|
Baylor Genetics
Accession: SCV005058300.1
First in ClinVar: Jun 17, 2024 Last updated: Jun 17, 2024 |
|
Comment:
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. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The glycine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has been observed in individual(s) with clinical features of hereditary breast and ovarian cancer syndrome (PMID: 21120943). ClinVar contains an entry for this variant (Variation ID: 808278). This variant is not present in population databases (ExAC no frequency). This sequence change replaces aspartic acid with glycine at codon 1482 of the BRCA1 protein (p.Asp1482Gly). The aspartic acid residue is moderately conserved and there is a moderate physicochemical difference between aspartic acid and glycine.
Comment:
The p.D1482G variant (also known as c.4445A>G), located in coding exon 12 of the BRCA1 gene, results from an A to G substitution at nucleotide position 4445. The aspartic acid at codon 1482 is replaced by glycine, an amino acid with similar properties. In one study, this variant was observed in 1/1525 unrelated patients who had BRCA1/2 genetic testing due to a personal and/or family history suspicious for Hereditary Breast and/or Ovarian Cancer (Caux-Moncoutier V et al. Hum. Mutat., 2011 Mar;32:325-34). This amino acid position is not well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.
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:
ACMG codes applied following ENIGMA VCEP rules: PM2_SUP
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. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The glycine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has been observed in individual(s) with clinical features of hereditary breast and ovarian cancer syndrome (PMID: 21120943). ClinVar contains an entry for this variant (Variation ID: 808278). This variant is not present in population databases (ExAC no frequency). This sequence change replaces aspartic acid with glycine at codon 1482 of the BRCA1 protein (p.Asp1482Gly). The aspartic acid residue is moderately conserved and there is a moderate physicochemical difference between aspartic acid and glycine.
Comment:
The p.D1482G variant (also known as c.4445A>G), located in coding exon 12 of the BRCA1 gene, results from an A to G substitution at nucleotide position 4445. The aspartic acid at codon 1482 is replaced by glycine, an amino acid with similar properties. In one study, this variant was observed in 1/1525 unrelated patients who had BRCA1/2 genetic testing due to a personal and/or family history suspicious for Hereditary Breast and/or Ovarian Cancer (Caux-Moncoutier V et al. Hum. Mutat., 2011 Mar;32:325-34). This amino acid position is not well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.
Citations for germline classification of this variant
Help| Title | Author | Journal | Year | Link |
|---|---|---|---|---|
| EMMA, a cost- and time-effective diagnostic method for simultaneous detection of point mutations and large-scale genomic rearrangements: application to BRCA1 and BRCA2 in 1,525 patients. | Caux-Moncoutier V | Human mutation | 2011 | PMID: 21120943 |
Text-mined citations for rs757726297 ...
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Record last updated Nov 03, 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.