Variant #0000016241 (NC_000019.9:g.36398134C>A, NM_003332.3:c.262G>T (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.36398134C>A
DNA change (hg38) g.35907232C>A
Published as G262T: E87X
ISCN -
DB-ID TYROBP_000007
Variant remarks 1 Japanese PLOSL patient (com-het)
Reference PubMed: Kuroda et al. 2007
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 2017-05-05 18:33:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYROBP NM_003332.3 +/+ 04 c.262G>T r.(262g>u) p.(Glu88*)


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