| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.108606794G>A | CA258650 | COL4A5 | c.2297G>A (p.Gly766Asp) n.1753G>A c.1973G>A (p.Gly658Asp) c.-33+3733G>A (n.-33+3733G>A) c.2312G>A (p.Gly771Asp) c.632G>A (p.Gly211Asp) | dbSNP |
| X | g.108606794G= | CA2450691460 | COL4A5 | c.2297G= (p.Gly766=) n.1753G= c.1973G= (p.Gly658=) c.-33+3733G= (n.-33+3733G=) c.2312G= (p.Gly771=) c.632G= (p.Gly211=) | dbSNP |