Variant #0000000034 (NC_000013.10:g.32893207T>A, NC_000013.10(NM_000059.3):c.68-7T>A (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.32893207T>A
Reference -
DB-ID BRCA2_000011
Frequency -
Average frequency (gnomAD v.2.1.1) 0.0029 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-12-05 08:48:15 +00:00 (UTC)
Date last edited 2017-12-05 10:57:27 +00:00 (UTC)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 -?/? 2i c.68-7T>A r.(=) p.(=)