Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108595557G>A | CA258482 | COL4A5 | c.1472G>A (p.Gly491Glu) n.928G>A c.1148G>A (p.Gly383Glu) c.1487G>A (p.Gly496Glu) c.-194G>A (n.-194G>A) | dbSNP COSMIC |
X | g.108595557G= | CA2450687744 | COL4A5 | c.1472G= (p.Gly491=) n.928G= c.1148G= (p.Gly383=) c.1487G= (p.Gly496=) c.-194G= (n.-194G=) | dbSNP |