| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.52451285C>T | CA122392 | TNNC1 | c.476G>A (p.Gly159Asp) | ClinVar dbSNP |
| 3 | g.52451285C>G | CA353164624 | TNNC1 | c.476G>C (p.Gly159Ala) | dbSNP |
| 3 | g.52451285C= | CA1364863550 | TNNC1 | c.476G= (p.Gly159=) | dbSNP |
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.52451285C>T | CA122392 | TNNC1 | c.476G>A (p.Gly159Asp) | ClinVar dbSNP |
| 3 | g.52451285C>G | CA353164624 | TNNC1 | c.476G>C (p.Gly159Ala) | dbSNP |
| 3 | g.52451285C= | CA1364863550 | TNNC1 | c.476G= (p.Gly159=) | dbSNP |