Variant #0001052910 (NC_000007.13:g.152357813del, NM_005431.1:c.96del (XRCC2))

Chromosome 7
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.152357813del
DNA change (hg38) -
Published as XRCC2(NM_005431.2):c.96del (p.(Phe32LeufsTer30)), XRCC2(NM_005431.2):c.96delT (p.F32Lfs*30)
ISCN -
DB-ID XRCC2_000033 See all 4 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
XRCC2 NM_005431.1 ?/. - c.96del - r.(?) p.(Phe32LeufsTer30)


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