| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.131890410G>T | CA256903 | ENPP1 | n.1108G>T c.2677G>T (p.Glu893Ter) c.*1514G>T (n.*1514G>T) c.1567G>T (p.Glu523Ter) | ClinVar dbSNP |
| 6 | g.131890410G= | CA1664283128 | ENPP1 | n.1108G= c.2677G= (p.Glu893=) c.*1514G= (n.*1514G=) c.1567G= (p.Glu523=) | dbSNP |