Variant #0000000058 (NC_000013.11:g.32337751A>G, BRCA2(NM_000059.3):c.3396A>G)

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32337751A>G
Published as -
Reference Toh GT et al.(2008)dbSNP
DB-ID BRCA2_000051 See all 2 reported entries
dbSNP ID rs1801406
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
BRCA2 NM_000059.3 -/. 11 c.3396A>G - r.(=) p.(=) - ClinVar