| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.46858425A>T | CA013996 | MYL3 | c.518T>A (p.Met173Lys) n.725T>A n.476T>A | ClinVar dbSNP |
| 3 | g.46858425A>G | CA352495476 | MYL3 | c.518T>C (p.Met173Thr) n.725T>C n.476T>C | ClinVar dbSNP |
| 3 | g.46858425A= | CA1362296542 | MYL3 | c.518T= (p.Met173=) n.725T= n.476T= | dbSNP |