Variant #0000351286 (NC_000017.10:g.56772522G>A, NM_058216.1:c.376G>A (RAD51C))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56772522G>A
DNA change (hg38) g.58695161G>A
Published as RAD51C(NM_002876.2):c.376G>A (p.(Ala126Thr)), RAD51C(NM_058216.1):c.376G>A (p.A126T), RAD51C(NM_058216.3):c.376G>A (p.A126T)
ISCN -
DB-ID RAD51C_000008 See all 15 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0035 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
TEX14 NM_001201457.1 -?/. - c.-3224C>T r.(?) p.(=) -
RAD51C NM_058216.1 -?/. - c.376G>A r.(?) p.(Ala126Thr) -


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