| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.108598808G>A | CA258565 | COL4A5 | c.1886G>A (p.Gly629Asp) n.1342G>A c.1562G>A (p.Gly521Asp) c.1901G>A (p.Gly634Asp) c.221G>A (p.Gly74Asp) | ClinVar dbSNP |
| X | g.108598808G= | CA2450688849 | COL4A5 | c.1886G= (p.Gly629=) n.1342G= c.1562G= (p.Gly521=) c.1901G= (p.Gly634=) c.221G= (p.Gly74=) | dbSNP |