Variant #0000016239 (NC_000019.9:g.36398432C>G, NM_003332.3:c.145G>C (TYROBP))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.36398432C>G
DNA change (hg38) g.35907530C>G
Published as -
ISCN -
DB-ID TYROBP_000005
Variant remarks 1 Portugese PLOSL family
Reference PubMed: Klünemann et al. 2005
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 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 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 ?/? 03 c.145G>C r.(145g>c) p.(Gly49Arg)


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