| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.46859573C>G | CA352496284 | MYL3 | c.383G>C (p.Gly128Ala) n.605G>C n.341G>C | ClinVar dbSNP |
| 3 | g.46859573C>T | CA351912 | MYL3 | c.383G>A (p.Gly128Asp) n.605G>A n.341G>A | ClinVar dbSNP gnomAD v4 |
| 3 | g.46859573C= | CA1362297128 | MYL3 | c.383G= (p.Gly128=) n.605G= n.341G= | dbSNP |
| 3 | g.46859573C>A | CA352496283 | MYL3 | c.383G>T (p.Gly128Val) n.605G>T n.341G>T | ClinVar dbSNP |