Variant #0000000031 (NC_000013.10:g.32912799T>C, NM_000059.3:c.4307T>C (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.32912799T>C
Reference -
DB-ID BRCA2_000010
Frequency -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-07-28 13:34:43 +00:00 (UTC)
Date last edited 2024-05-13 11:23:37 +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.4307T>C r.(?) p.(Ile1436Thr)