Variant #0000868903 (NC_000019.9:g.17449383G>A, NM_032620.3:c.424G>A (GTPBP3))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.17449383G>A
DNA change (hg38) g.17338574G>A
Published as -
ISCN -
DB-ID GTPBP3_000008 See all 3 reported entries
Variant remarks functional analysis by expression cloning HEK293 cells; reduced stability, no yeast complementation, normal hMTO1 interaction
Reference PubMed: Peng 2021
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-05-26 10:28:42 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GTPBP3 NM_032620.3 +/. - c.424G>A - p.Glu142Lys


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