Variant #0000000013 (NC_000013.10:g.32913562A>C, NM_000059.3:c.5070A>C (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.32913562A>C
Reference -
DB-ID BRCA2_000004
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00021 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 09:36:09 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA2 NM_000059.3 ?/? 11 c.5070A>C r.(?) p.(Lys1690Asn)