Variant #0000000029 (NC_000013.11:g.32338137C>G, NM_000059.3:c.3782C>G (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.32338137C>G
Published as -
Reference E Thirthagiri et al. (2008)dbSNP
DB-ID BRCA2_000024
dbSNP ID rs276174836
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
Date created 2017-11-20 08:02:24 +08:00 (CST)
Date last edited 2021-09-09 12:40:32 +08:00 (CST)
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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.3782C>G - r.(?) p.(Ser1261Cys) - ClinVar