| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55154095G>A | CA021738 | TNNI3 | c.484C>T (p.Arg162Trp) c.517C>T (p.Arg173Trp) n.483C>T c.409C>T (p.Arg137Trp) n.312C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.55154095G>C | CA407440362 | TNNI3 | c.484C>G (p.Arg162Gly) c.517C>G (p.Arg173Gly) n.483C>G c.409C>G (p.Arg137Gly) n.312C>G | ClinVar dbSNP gnomAD v4 |
| 19 | g.55154095G>T | CA508989406 | TNNI3 | c.484C>A (p.Arg162=) c.517C>A (p.Arg173=) n.483C>A c.409C>A (p.Arg137=) n.312C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |