Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108595574G>T | CA258486 | COL4A5 | c.1489G>T (p.Gly497Cys) n.945G>T c.1165G>T (p.Gly389Cys) c.1504G>T (p.Gly502Cys) c.-177G>T (n.-177G>T) | dbSNP |
X | g.108595574G= | CA2450687756 | COL4A5 | c.1489G= (p.Gly497=) n.945G= c.1165G= (p.Gly389=) c.1504G= (p.Gly502=) c.-177G= (n.-177G=) | dbSNP |