Variant #0000868906 (NC_000019.9:g.[17449940G>A;17450398G>C], NM_032620.3:c.[673G>A;964G>C] (GTPBP3))
| Chromosome |
19 |
| Allele |
Parent #1 |
| 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.[17449940G>A;17450398G>C] |
| DNA change (hg38) |
g.[17339131G>A;17339589G>C] |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GTPBP3_000017 |
| Variant remarks |
functional analysis by expression cloning HEK293 cells; normal stability, 0.13 GTPase activityreduced 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 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-05-26 10:28:42 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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