Variant #0000868905 (NC_000019.9:g.17449443G>C, NM_032620.3:c.484G>C (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.17449443G>C
DNA change (hg38) g.17338634G>C
Published as -
ISCN -
DB-ID GTPBP3_000014 See all 2 reported entries
Variant remarks functional analysis by expression cloning HEK293 cells; normal stability, 0.09 GTPase activityreduced stability, no yeast complementation, reduced 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GTPBP3 NM_032620.3 +/. - c.484G>C - p.Ala162Pro


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