Variant #0000000032 (NC_000017.10:g.41199741G>C, NC_000017.10(NM_007294.3):c.5407-21C>G (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.41199741G>C
Reference -
DB-ID BRCA1_000004
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-08-18 09:38:07 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRCA1 NM_007294.3 ./? 22 c.5407-21C>G r.(=) p.(=)