| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55154068C>T | CA021791 | TNNI3 | c.511G>A (p.Ala171Thr) c.544G>A (p.Ala182Thr) n.510G>A c.436G>A (p.Ala146Thr) n.339G>A | ClinVar dbSNP gnomAD v4 |
| 19 | g.55154068C= | CA2343273733 | TNNI3 | c.511G= (p.Ala171=) c.544G= (p.Ala182=) n.510G= c.436G= (p.Ala146=) n.339G= | dbSNP |
| 19 | g.55154068C>G | CA407440301 | TNNI3 | c.511G>C (p.Ala171Pro) c.544G>C (p.Ala182Pro) n.510G>C c.436G>C (p.Ala146Pro) n.339G>C | dbSNP |