Variant #0000578986 (NC_000006.11:g.132172368A>C, NM_006208.2:c.517A>C (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.132172368A>C |
| DNA change (hg38) |
g.131851228A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ENPP1_000035 See all 7 reported entries |
| Variant remarks |
cDNA expression cloning HEK293/COS7 cells, 0.66 NPP enzyme activity/0.63 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) |
0.19363 View details |
| Owner |
Yvonne Nitschke |
| Database submission license |
No license selected |
| Created by |
Yvonne Nitschke |
| Date created |
2018-10-30 16:41:04 +01:00 (CET) |
| Date last edited |
2020-06-22 10:23:54 +02:00 (CEST) |

Variant on transcripts
|