| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154032252C>T | CA16043705 | MECP2 | c.332G>A (p.Arg111Lys) c.368G>A (p.Arg123Lys) c.*386G>A (n.*386G>A) n.2680G>A c.320G>A (p.Arg107Lys) c.53G>A (p.Arg18Lys) c.-229G>A (n.-229G>A) | ClinVar dbSNP |
| X | g.154032252C>G | CA415176724 | MECP2 | c.332G>C (p.Arg111Thr) c.368G>C (p.Arg123Thr) c.*386G>C (n.*386G>C) n.2680G>C c.320G>C (p.Arg107Thr) c.53G>C (p.Arg18Thr) c.-229G>C (n.-229G>C) | ClinVar dbSNP |
| X | g.154032252C= | CA2466571530 | MECP2 | c.332G= (p.Arg111=) c.368G= (p.Arg123=) c.*386G= (n.*386G=) n.2680G= c.320G= (p.Arg107=) c.53G= (p.Arg18=) c.-229G= (n.-229G=) | dbSNP |