Variant #0000572114 (NC_000022.10:g.41257393C>A, NC_000022.10(NM_022098.3):c.64+4144C>A (XPNPEP3))

Chromosome 22
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.41257393C>A
DNA change (hg38) g.40861389C>A
Published as DNAJB7(NM_145174.1):c.606G>T (p.(Lys202Asn))
ISCN -
DB-ID DNAJB7_000003
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) 0.0171 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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ST13 NM_003932.3 -?/. - c.-4849G>T r.(?) p.(=)
XPNPEP3 NM_022098.3 -?/. - c.64+4144C>A r.(=) p.(=)
DNAJB7 NM_145174.1 -?/. - c.606G>T r.(?) p.(Lys202Asn)


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