Variant #0000000251 (NC_000013.10:g.32914126C>T, NM_000059.3:c.5634C>T (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.32914126C>T
Reference -
DB-ID BRCA2_000034
Frequency -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
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 13:38:12 +00:00 (UTC)
Date last edited 2024-05-13 11:17:44 +00:00 (UTC)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 -?/-? 11 c.5634C>T r.(=) p.(=)