Variant #0000003664 (NC_000017.11:g.43124028_43124029delCT, NM_007294.3:c.68_69delAG (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg38 / GRCh38) g.43124028_43124029delCT
Reference -
DB-ID BRCA1_000010 See all 18 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florencia Petracchi-CEMIC
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
Date created 2018-02-05 17:06:50 -02:00 (-02)
Date last edited 2024-01-22 15:41:45 -02:00 (-02)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Review status     
BRCA1 NM_007294.3 +/+ 2 c.68_69delAG r.(?) p.(Glu23Valfs*17) Hetero MSH2 -



Screenings

Stop! No screenings found!