Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.58975061A>G | CA150721 | PDE4D | c.1841T>C (p.Ile614Thr) c.2033T>C (p.Ile678Thr) c.1703T>C (p.Ile568Thr) c.1885T>C (n.1885T>C) c.1160T>C (p.Ile387Thr) c.1127T>C (p.Ile376Thr) c.1625T>C (p.Ile542Thr) c.1667T>C (p.Ile556Thr) c.1850T>C (p.Ile617Thr) c.1643T>C (p.Ile548Thr) n.1769T>C c.1640T>C (p.Ile547Thr) c.1361T>C (p.Ile454Thr) c.1997T>C (p.Ile666Thr) c.1820T>C (p.Ile607Thr) c.1613T>C (p.Ile538Thr) c.1592T>C (p.Ile531Thr) c.1529T>C (p.Ile510Thr) c.1265T>C (p.Ile422Thr) c.1835T>C (p.Ile612Thr) | ClinVar dbSNP |
5 | g.58975061A= | CA1549121707 | PDE4D | c.1841T= (p.Ile614=) c.2033T= (p.Ile678=) c.1703T= (p.Ile568=) c.1885T= (n.1885T=) c.1160T= (p.Ile387=) c.1127T= (p.Ile376=) c.1625T= (p.Ile542=) c.1667T= (p.Ile556=) c.1850T= (p.Ile617=) c.1643T= (p.Ile548=) n.1769T= c.1640T= (p.Ile547=) c.1361T= (p.Ile454=) c.1997T= (p.Ile666=) c.1820T= (p.Ile607=) c.1613T= (p.Ile538=) c.1592T= (p.Ile531=) c.1529T= (p.Ile510=) c.1265T= (p.Ile422=) c.1835T= (p.Ile612=) | dbSNP |