Variant #0000950959 (NC_000017.10:g.56772370dup, NM_058216.1:c.224dup (RAD51C))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.56772370dup
DNA change (hg38) -
Published as RAD51C(NM_058216.1):c.224dupA (p.Y75*), RAD51C(NM_058216.3):c.224dupA (p.Y75*)
ISCN -
DB-ID RAD51C_000029 See all 6 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) Retrieve
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
TEX14 NM_001201457.1 +/. - c.-3072dup r.(?) p.(=) -
RAD51C NM_058216.1 +/. - c.224dup r.(?) p.(Tyr75*) -


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