Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.58975061A>GCA150721PDE4Dc.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
5g.58975061A=CA1549121707PDE4Dc.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

Number of alleles fetched