Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.8989G>A | CA414801774 | MT-ATP6 | c.463G>A (p.Ala155Thr) | ClinVar dbSNP |
MT | m.8989G>C | CA345922 | MT-ATP6 | c.463G>C (p.Ala155Pro) | ClinVar dbSNP |
MT | m.8989G= | CA2499566034 | MT-ATP6 | c.463G= (p.Ala155=) | dbSNP |