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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 +/+ 2 c.65T>C r.(?) p.(Leu22Ser) -