Variant #0000000056 (NC_000013.11:g.32336584T>C, NM_000059.3:c.2229T>C (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.32336584T>C
Published as -
Reference Toh GT et al.(2008), dbSNP, ClinVar
DB-ID BRCA2_000049 See all 2 reported entries
dbSNP ID rs1801499
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 03:46:30 +08:00 (CST)
Date last edited 2021-09-09 13:02:33 +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 -/. 11 c.2229T>C - r.(=) p.(=) - ClinVar