| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.131860388G>C | CA365667448 | ENPP1 | c.797G>C (p.Gly266Ala) c.414G>C c.288G>C | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.131860388G>T | CA123290 | ENPP1 | c.797G>T (p.Gly266Val) c.414G>T c.288G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.131860388G= | CA1664259047 | ENPP1 | c.797G= (p.Gly266=) c.414G= c.288G= | dbSNP |