Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108591627G>A | CA258471 | COL4A5 | c.1406G>A (p.Gly469Glu) n.862G>A c.1082G>A (p.Gly361Glu) c.1421G>A (p.Gly474Glu) c.-304G>A (n.-304G>A) | dbSNP |
X | g.108591627G= | CA2450686587 | COL4A5 | c.1406G= (p.Gly469=) n.862G= c.1082G= (p.Gly361=) c.1421G= (p.Gly474=) c.-304G= (n.-304G=) | dbSNP |