Variant #0000000152 (NC_000017.11:g.43093449G>A, BRCA1(NM_007294.3):c.2082C>T)

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.43093449G>A
Published as -
Reference E Thirthagiri et al. (2008), dbSNP ,ClinVar
DB-ID BRCA1_000040 See all 7 reported entries
dbSNP ID rs1799949
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 -/? 11 c.2082C>T - r.(=) p.(=) - ClinVar