| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55151905C>T | CA021922 | TNNI3 | c.562G>A (p.Val188Met) c.595G>A (p.Val199Met) n.561G>A c.487G>A (p.Val163Met) n.390G>A | ClinVar dbSNP gnomAD v4 |
| 19 | g.55151905C>A | CA021928 | TNNI3 | c.562G>T (p.Val188Leu) c.595G>T (p.Val199Leu) n.561G>T c.487G>T (p.Val163Leu) n.390G>T | ClinVar dbSNP gnomAD v4 |
| 19 | g.55151905C= | CA2343272654 | TNNI3 | c.562G= (p.Val188=) c.595G= (p.Val199=) n.561G= c.487G= (p.Val163=) n.390G= | dbSNP |
| 19 | g.55151905C>G | CA407439663 | TNNI3 | c.562G>C (p.Val188Leu) c.595G>C (p.Val199Leu) n.561G>C c.487G>C (p.Val163Leu) n.390G>C | dbSNP gnomAD v4 |