Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108591135G>A | CA258441 | COL4A5 | c.1243G>A (p.Gly415Arg) n.699G>A c.919G>A (p.Gly307Arg) c.1258G>A (p.Gly420Arg) c.-467G>A (n.-467G>A) | dbSNP |
X | g.108591135G= | CA2450686415 | COL4A5 | c.1243G= (p.Gly415=) n.699G= c.919G= (p.Gly307=) c.1258G= (p.Gly420=) c.-467G= (n.-467G=) | dbSNP |