Variant #0000016235 (NC_000019.9:g.36399129A>G, NM_003332.3:c.2T>C (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.36399129A>G
DNA change (hg38) g.35908227A>G
Published as T>C point mutation disrupting the start codon
ISCN -
DB-ID TYROBP_000001
Variant remarks 2 Japanese PLOSL patients (hom)
Reference PubMed: Kondo et al.2002
ClinVar ID -
dbSNP ID rs104894732
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 +/+ 01b c.2T>C r.(2u>c) p.0


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