| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.52452167C>A | CA10588371 | TNNC1 | c.141G>T (p.Met47Ile) c.9G>T (p.Met3Ile) | ClinVar dbSNP |
| 3 | g.52452167C= | CA1364863987 | TNNC1 | c.141G= (p.Met47=) c.9G= (p.Met3=) | dbSNP |
| 3 | g.52452167C>T | CA353168720 | TNNC1 | c.141G>A (p.Met47Ile) c.9G>A (p.Met3Ile) | ClinVar dbSNP |