Variant #0000000010 (NC_000013.11:g.32336991_32336992delCT, BRCA2(NM_000059.3):c.2636_2637delCT)

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.32336991_32336992delCT
Published as -
Reference E Thirthagiri et al. (2008), dbSNP, ClinVar
DB-ID BRCA2_000005 See all 2 reported entries
dbSNP ID rs276174826
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
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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.2636_2637delCT - r.(?) p.(Ser879*) - ClinVar