Variant #0000000019 (NC_000017.10:g.33430313T>C, NM_002878.3:c.698A>G (RAD51D))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.33430313T>C
Reference -
DB-ID RAD51D_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00947 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-05-15 09:58:24 +00:00 (UTC)
Date last edited 2023-07-18 10:56:41 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51D NM_002878.3 -?/-? 8 c.698A>G r.(?) p.(Glu233Gly)