Variant #0000011735 (NC_000017.11:g.33430511G>T, RAD51D(NM_002878.4):c.629C>A)

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.33430511G>T
Reference -
DB-ID RAD51D_000025 See all 4 reported entries
dbSNP ID rs376855484
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Guillermo Alberto-Instituto Fleming
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Protein     

Zygosity     

Co_ocurrence     

RNA change     

Review status     
RAD51D NM_002878.4 ?/? 3 c.629C>A p.(Ala210Glu) Hetero no r.(?) -