Variant #0000578987 (NC_000006.11:g.132173341T>A, NM_006208.2:c.583T>A (ENPP1))
Chromosome |
6 |
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.132173341T>A |
DNA change (hg38) |
g.131852201T>A |
Published as |
- |
ISCN |
- |
DB-ID |
ENPP1_000029 See all 3 reported entries |
Variant remarks |
cDNA expression cloning HEK293/COS7 cells, no NPP enzyme activity/PPi generation, no localisation plasma membrane |
Reference |
PubMed: Stella 2016 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Yvonne Nitschke |
Database submission license |
No license selected |
Created by |
Yvonne Nitschke |
Date created |
2016-07-15 10:44:28 +02:00 (CEST) |
Date last edited |
2020-06-22 10:23:58 +02:00 (CEST) |

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