Variant #0000578975 (NC_000006.11:g.132193216A>G, NM_006208.2:c.1412A>G (ENPP1))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.132193216A>G |
| DNA change (hg38) |
g.131872076A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ENPP1_000012 See all 14 reported entries |
| Variant remarks |
cDNA expression cloning HEK293/COS7 cells, 0.43 NPP enzyme activity/0.67 PPi generation, 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) |
8.0E-5 View details |
| 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 10:24:04 +02:00 (CEST) |

Variant on transcripts
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