Variant #0000000054 (NC_000013.11:g.32332820C>T, NM_000059.3:c.1342C>T (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32332820C>T
Published as -
Reference Toh GT et al.(2008), dbSNP, ClinVar
DB-ID BRCA2_000047
dbSNP ID rs80358422
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2017-11-21 03:37:32 +08:00 (CST)
Date last edited 2021-09-09 12:49:09 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
BRCA2 NM_000059.3 ?/. 10 c.1342C>T - r.(?) p.(Arg448Cys) - ClinVar