Variant #0000000009 (NC_000017.10:g.56809910_56809912del, NC_000017.10(NM_058216.2):c.1026+5_1026+7del (RAD51C))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.56809910_56809912del
Reference -
DB-ID RAD51C_000001
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-05-15 09:17:29 +00:00 (UTC)
Date last edited 2023-07-18 10:52:08 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51C NM_058216.2 +?/+? 8 c.1026+5_1026+7del r.spl? p.?