Variant #0000881494 (NC_000006.11:g.132172407G>C, NM_006208.2:c.556G>C (ENPP1))
| Chromosome |
6 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.132172407G>C |
| DNA change (hg38) |
g.131851267G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ENPP1_000099 See all 5 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Mercurio 2022, Journal: Mercurio 2022 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-10-23 14:20:36 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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