| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.48685634G>T | CA16608484 | WAS | n.393+1G>T c.360+1G>T (n.360+1G>T) n.395+1G>T n.386+1G>T | ClinVar dbSNP |
| X | g.48685634G>C | CA412867292 | WAS | n.393+1G>C c.360+1G>C (n.360+1G>C) n.395+1G>C n.386+1G>C | ClinVar dbSNP |
| X | g.48685634G>A | CA16609187 | WAS | n.393+1G>A c.360+1G>A (n.360+1G>A) n.395+1G>A n.386+1G>A | ClinVar dbSNP |