Variant #0000000250 (NC_000013.10:g.32913452T>G, NM_000059.3:c.4960T>G (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.32913452T>G
Reference -
DB-ID BRCA2_000033
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-27 13:37:26 +00:00 (UTC)
Date last edited 2024-05-13 11:24:26 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 ?/-? 11 c.4960T>G r.(?) p.(Cys1654Gly)