Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108625732G>T | CA258794 | COL4A5 | c.3044G>T (p.Gly1015Val) n.2500G>T c.277G>T c.2720G>T (p.Gly907Val) c.617G>T (p.Gly206Val) c.3059G>T (p.Gly1020Val) c.1379G>T (p.Gly460Val) | dbSNP |
X | g.108625732G= | CA2450697896 | COL4A5 | c.3044G= (p.Gly1015=) n.2500G= c.277G= c.2720G= (p.Gly907=) c.617G= (p.Gly206=) c.3059G= (p.Gly1020=) c.1379G= (p.Gly460=) | dbSNP |