Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.11914G>C | CA337099336 | MT-ND4 | c.1155G>C (p.Thr385=) | dbSNP |
MT | m.11914G>A | CA337099334 | MT-ND4 | c.1155G>A (p.Thr385=) | ClinVar dbSNP COSMIC |
MT | m.11914G= | CA2499567330 | MT-ND4 | c.1155G= (p.Thr385=) | dbSNP |