| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.108601893G>T | CA258602 | COL4A5 | c.2050G>T (p.Gly684Ter) n.1506G>T c.1726G>T (p.Gly576Ter) c.2065G>T (p.Gly689Ter) c.385G>T (p.Gly129Ter) | dbSNP |
| X | g.108601893G= | CA2450689938 | COL4A5 | c.2050G= (p.Gly684=) n.1506G= c.1726G= (p.Gly576=) c.2065G= (p.Gly689=) c.385G= (p.Gly129=) | dbSNP |