| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.14178T>C | CA337099941 | MT-ND6 | c.496A>G (p.Ile166Val) | ClinVar dbSNP |
| MT | m.14178T= | CA2499568357 | MT-ND6 | c.496A= (p.Ile166=) | dbSNP |
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.14178T>C | CA337099941 | MT-ND6 | c.496A>G (p.Ile166Val) | ClinVar dbSNP |
| MT | m.14178T= | CA2499568357 | MT-ND6 | c.496A= (p.Ile166=) | dbSNP |