| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.16182910T>C | CA278648350 | ABCC6 | c.1964A>G (p.Gln655Arg) n.2040-985A>G c.1622A>G (p.Gln541Arg) n.2199A>G n.2200A>G n.2001A>G c.2000A>G (p.Gln667Arg) n.2145A>G | ClinVar dbSNP |
| 16 | g.16182910T= | CA2210149777 | ABCC6 | c.1964A= (p.Gln655=) n.2040-985A= c.1622A= (p.Gln541=) n.2199A= n.2200A= n.2001A= c.2000A= (p.Gln667=) n.2145A= | dbSNP |