Variant #0000016237 (NC_000019.9:g.36396774_36402030del, NC_000019.9(NM_003332.3):c.-2900_277-1238del (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.36396774_36402030del
DNA change (hg38) g.35905872_35911128del
Published as deletion exons 1-4; PLOSL Fin
ISCN -
DB-ID TYROBP_000003
Variant remarks Major Finnish PLOSL mutation: 25 Finnish PLOSL patients (hom). Also 1 Swedish PLOSL family (hom), 1 Norwegian PLOSL family (hom) and 1 Brazilian PLOSL family.
Reference PubMed: Paloneva 2000, PubMed: Paloneva 2002
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/120 FIN CON
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 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYROBP NM_003332.3 +/+ _1b_4i c.-2900_277-1238del r.0 p.0


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.