Variant #0000569705 (NC_000020.10:g.42789001_42789002del, NM_020433.4:c.426_427del (JPH2))

Chromosome 20
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.42789001_42789002del
DNA change (hg38) g.44160361_44160362del
Published as JPH2(NM_020433.5):c.426_427delAG (p.V143Tfs*98)
ISCN -
DB-ID JPH2_000149
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JPH2 NM_020433.4 +/. - c.426_427del r.(?) p.(Val143ThrfsTer98)


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