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 International |
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) |

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