Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.15884G>A | CA170530 | MT-CYB | c.1138G>A (p.Ala380Thr) | ClinVar dbSNP |
MT | m.15884G>C | CA10586049 | MT-CYB | c.1138G>C (p.Ala380Pro) | ClinVar dbSNP |
MT | m.15884G= | CA2499569271 | MT-CYB | c.1138G= (p.Ala380=) | dbSNP |