Variant #0000000014 (NC_000013.10:g.32972626A>T, NM_000059.3:c.9976A>T (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.32972626A>T
Reference -
DB-ID BRCA2_000005
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00658 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-05-15 09:39:14 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 ?/? 27 c.9976A>T r.(?) p.(Lys3326*)