Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108601450G>C | CA258592 | COL4A5 | c.2006G>C (p.Gly669Ala) n.1462G>C c.1682G>C (p.Gly561Ala) c.2021G>C (p.Gly674Ala) c.341G>C (p.Gly114Ala) | dbSNP |
X | g.108601450G= | CA2450689753 | COL4A5 | c.2006G= (p.Gly669=) n.1462G= c.1682G= (p.Gly561=) c.2021G= (p.Gly674=) c.341G= (p.Gly114=) | dbSNP |