| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.10449495A>G | CA255551 | MID1 | c.1877T>C (p.Leu626Pro) c.1763T>C (p.Leu588Pro) c.1769T>C (p.Leu590Pro) c.1010T>C (p.Leu337Pro) c.2030T>C (p.Leu677Pro) c.*118T>C (n.*118T>C) n.827T>C c.1916T>C (p.Leu639Pro) | ClinVar dbSNP |
| X | g.10449495A= | CA2415269836 | MID1 | c.1877T= (p.Leu626=) c.1763T= (p.Leu588=) c.1769T= (p.Leu590=) c.1010T= (p.Leu337=) c.2030T= (p.Leu677=) c.*118T= (n.*118T=) n.827T= c.1916T= (p.Leu639=) | dbSNP |