Variant #0001068417 (NC_000022.10:g.41305124A>G, NC_000022.10(NM_022098.3):c.856-2A>G (XPNPEP3))

Chromosome 22
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.41305124A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID DNAJB7_000011 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs149609214
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-20 10:13:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XPNPEP3 NM_022098.3 +/. - c.856-2A>G r.(?) p.(?)


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