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

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
Date created 2017-11-27 03:24:19 +08:00 (CST)
Date last edited 2021-09-12 13:18:24 +08:00 (CST)
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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