Variant #0000000006 (NC_000013.11:g.32319271_32319272delCT, NM_000059.3:c.262_263delCT (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.32319271_32319272delCT
Published as -
Reference E Thirthagiri et al. (2008), dbSNP, ClinVar
DB-ID BRCA2_000001 See all 4 reported entries
dbSNP ID rs276174825
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 2017-11-19 08:39:29 +08:00 (CST)
Date last edited 2021-09-09 12:30:33 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
BRCA2 NM_000059.3 +/. 13 c.262_263delCT - r.(?) p.(Leu88Alafs*12) - ClinVar