| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.108577953G>A | CA258289 | COL4A5 | c.611G>A (p.Gly204Asp) c.287G>A (p.Gly96Asp) c.626G>A (p.Gly209Asp) | ClinVar dbSNP |
| X | g.108577953G>T | CA258292 | COL4A5 | c.611G>T (p.Gly204Val) c.287G>T (p.Gly96Val) c.626G>T (p.Gly209Val) | dbSNP |
| X | g.108577953G= | CA2450682168 | COL4A5 | c.611G= (p.Gly204=) c.287G= (p.Gly96=) c.626G= (p.Gly209=) | dbSNP |