Variant #0000016238 (NC_000019.9:g.36398436del, NM_003332.3:c.141del (TYROBP))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36398436del
DNA change (hg38) g.35907534del
Published as V48X; PLOSL Jpn
ISCN -
DB-ID TYROBP_000004
Variant remarks 9 Japanese PLOSL patients (most hom)
Reference PubMed: Paloneva et al. 2000, {PMID:Kuroda et al. 2007:17125796), PubMed: Kondo et al. 2002, PubMed: Klünemann et al. 2005, PubMed: Nakamagoe et al. 2011
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-11-13 16:18:18 +01:00 (CET)
Date last edited 2020-07-15 17:36:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYROBP NM_003332.3 +/+ 03 c.141del r.(?) p.0


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