| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.108601467G>A | CA258595 | COL4A5 | c.2023G>A (p.Gly675Ser) n.1479G>A c.1699G>A (p.Gly567Ser) c.2038G>A (p.Gly680Ser) c.358G>A (p.Gly120Ser) | ClinVar dbSNP |
| X | g.108601467G= | CA2450689761 | COL4A5 | c.2023G= (p.Gly675=) n.1479G= c.1699G= (p.Gly567=) c.2038G= (p.Gly680=) c.358G= (p.Gly120=) | dbSNP |