| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.52452217C>A | CA130608 | TNNC1 | c.91G>T (p.Ala31Ser) c.-42G>T (n.-42G>T) | ClinVar dbSNP |
| 3 | g.52452217C>T | CA297310 | TNNC1 | c.91G>A (p.Ala31Thr) c.-42G>A (n.-42G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.52452217C= | CA1364864004 | TNNC1 | c.91G= (p.Ala31=) c.-42G= (n.-42G=) | dbSNP |