Variant #0000573439 (NC_000023.10:g.128895150C>T, NM_003399.5:c.1501C>T (XPNPEP2))

Chromosome X
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.128895150C>T
DNA change (hg38) g.129761174C>T
Published as XPNPEP2(NM_003399.5):c.1501C>T (p.(Arg501Ter))
ISCN -
DB-ID XPNPEP2_000022
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) 0.0001 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-21 09:46:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XPNPEP2 NM_003399.5 -?/. - c.1501C>T r.(?) p.(Arg501Ter)


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