| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.9804G>A | CA340930 | MT-CO3 | c.598G>A (p.Ala200Thr) | ClinVar dbSNP |
| MT | m.9804G>C | CA414803748 | MT-CO3 | c.598G>C (p.Ala200Pro) | ClinVar dbSNP |
| MT | m.9804G>T | CA414803749 | MT-CO3 | c.598G>T (p.Ala200Ser) | ClinVar dbSNP |
| MT | m.9804G= | CA2499566471 | MT-CO3 | c.598G= (p.Ala200=) | dbSNP |