| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.13513G>C | CA414818324 | MT-ND5 | c.1177G>C (p.Asp393His) | dbSNP |
| MT | m.13513G>A | CA120632 | MT-ND5 | c.1177G>A (p.Asp393Asn) | ClinVar dbSNP |
| MT | m.13513G>T | CA414818326 | MT-ND5 | c.1177G>T (p.Asp393Tyr) | dbSNP |
| MT | m.13513G= | CA2499568034 | MT-ND5 | c.1177G= (p.Asp393=) | dbSNP |