Variant #0000000121 (NC_000017.11:g.43099851_43099852delAG, BRCA1(NM_007294.3):c.470_471delCT)

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.43099851_43099852delAG
Published as -
Reference E Thirthagiri et al. (2008)dbSNP
DB-ID BRCA1_000009 See all 3 reported entries
dbSNP ID rs80357887
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
BRCA1 NM_007294.3 +/? 8 c.470_471delCT - r.(?) p.(Ser157*) - ClinVar