Variant #0000191038 (NC_000017.10:g.41276049A>G, BRCA1(NM_007294.3):c.65T>C)
Chromosome |
17 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic (dominant) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41276049A>G |
DNA change (hg38) |
g.43124032A>G |
Published as |
- |
ISCN |
- |
DB-ID |
BRCA1_000013 See all 6 reported entries |
Variant remarks |
IARC class based on posterior probability from multifactorial likelihood analysis, thresholds for class as per Plon 2008 (PMID:18951446). Class 5 based on posterior probability = 0.99 |
Reference |
ENIGMA classification criteria, Details in BRCA database Tavtigian lab, PubMed: Lindor 2012 |
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 |
No license selected |
Created by |
ENIGMA consortium |

Variant on transcripts
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