Variant #0001072073 (NC_000017.10:g.56772309G>A, NM_058216.1:c.163G>A (RAD51C))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.56772309G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID RAD51C_000299
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1555593472
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-08 14:49:02 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
RAD51C NM_058216.1 ?/. - c.163G>A r.(?) p.(Ala55Thr) -


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