Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108591178G>A | CA258453 | COL4A5 | c.1286G>A (p.Gly429Glu) n.742G>A c.962G>A (p.Gly321Glu) c.1301G>A (p.Gly434Glu) c.-424G>A (n.-424G>A) | ClinVar dbSNP |
X | g.108591178G= | CA2450686432 | COL4A5 | c.1286G= (p.Gly429=) n.742G= c.962G= (p.Gly321=) c.1301G= (p.Gly434=) c.-424G= (n.-424G=) | dbSNP |