Variant #0000000086 (NC_000013.11:g.32337464C>T, NM_000059.3:c.3109C>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.32337464C>T
Published as -
Reference Toh GT et al.(2008), dbSNP ,ClinVar
DB-ID BRCA2_000054 See all 6 reported entries
dbSNP ID rs80358557
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 15:13:26 +08:00 (CST)
Date last edited 2021-09-09 13:16:22 +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.3109C>T - r.(?) p.(Gln1037*) - ClinVar