Variant #0000016240 (NC_000019.9:g.36398422_36398423ins42, NM_003332.3:c.154_155ins42 (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.36398422_36398423ins42
DNA change (hg38) -
Published as 154-155ins42nt, Ins of 14 aa
ISCN -
DB-ID TYROBP_000006
Variant remarks 1 Scottish 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) 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 +/+ 03 c.154_155ins42 r.(154_155ins42) p.?


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