Variant #0000191077 (NC_000017.10:g.41279882A>G, NM_007294.3:c.-2614T>C (BRCA1))
Chromosome |
17 |
Allele |
Parent #1 |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41279882A>G |
DNA change (hg38) |
g.43127865A>G |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA1_004601 |
Variant remarks |
Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.33 (Asian), 0.22 (African), 0.36 (European), derived from 1000 genomes (2012-04-30). |
Reference |
ENIGMA classification criteria |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
ENIGMA consortium |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
ENIGMA consortium |
Date created |
2015-12-01 12:00:00 +01:00 (CET) |
Date last edited |
2024-07-10 13:41:19 +02:00 (CEST) |

Variant on transcripts
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