Variant #0001022230 (NC_000010.10:g.97599449A>G, NM_001776.5:c.146A>G (ENTPD1))
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.97599449A>G |
DNA change (hg38) |
g.95839692A>G |
Published as |
- |
ISCN |
- |
DB-ID |
C10orf131_000010 See all 2 reported entries |
Variant remarks |
in vitro analysis 293T cells mini-gene exon trapping assay: no effect on RNA |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Tjakko van Ham |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2024-11-05 16:15:00 +01:00 (CET) |
Date last edited |
N/A |

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