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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-05 16:15:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENTPD1 NM_001776.5 ?/. 3 c.146A>G r.146A>G p.Tyr49Cys


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