Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108597489G>C | CA258523 | COL4A5 | c.1700G>C (p.Gly567Ala) n.1156G>C c.1376G>C (p.Gly459Ala) c.1715G>C (p.Gly572Ala) c.35G>C (p.Gly12Ala) | dbSNP |
X | g.108597489G= | CA2450688382 | COL4A5 | c.1700G= (p.Gly567=) n.1156G= c.1376G= (p.Gly459=) c.1715G= (p.Gly572=) c.35G= (p.Gly12=) | dbSNP |