| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.10688G>C | CA913164281 | MT-ND4L | c.219G>C (p.Val73=) | dbSNP |
| MT | m.10688G>A | CA337098956 | MT-ND4L | c.219G>A (p.Val73=) | ClinVar dbSNP |
| MT | m.10688G>T | CA913164280 | MT-ND4L | c.219G>T (p.Val73=) | dbSNP |
| MT | m.10688G= | CA2499566897 | MT-ND4L | c.219G= (p.Val73=) | dbSNP |