Variant #0000191265 (NC_000013.10:g.32900377A>G, NC_000013.10(NM_000059.3):c.476-2A>G (BRCA2))

Chromosome 13
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.32900377A>G
DNA change (hg38) g.32326240A>G
Published as -
ISCN -
DB-ID BRCA2_000031 See all 15 reported entries
Variant remarks Insufficient evidence to determine clinical significance. Variant allele produces r.476_516del AND full-length transcripts.,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 = 1
Reference ENIGMA classification criteria, Details in BRCA database Tavtigian lab, PubMed: Colombo 2013, 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 Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ENIGMA consortium
Date created 2015-10-08 12:00:00 +02:00 (CEST)
Date last edited 2025-06-09 06:04:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +?/+? 5i c.476-2A>G r.spl p.? -


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