Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.58975718T>GCA128856PDE4Dc.1760A>C (p.Glu587Ala)
c.1952A>C (p.Glu651Ala)
c.1622A>C (p.Glu541Ala)
c.1804A>C (n.1804A>C)
c.1079A>C (p.Glu360Ala)
c.1046A>C (p.Glu349Ala)
c.1544A>C (p.Glu515Ala)
c.1586A>C (p.Glu529Ala)
c.1769A>C (p.Glu590Ala)
c.1562A>C (p.Glu521Ala)
n.1688A>C
c.1559A>C (p.Glu520Ala)
c.1280A>C (p.Glu427Ala)
c.1916A>C (p.Glu639Ala)
c.1739A>C (p.Glu580Ala)
c.1532A>C (p.Glu511Ala)
c.1511A>C (p.Glu504Ala)
c.1448A>C (p.Glu483Ala)
c.1184A>C (p.Glu395Ala)
c.1754A>C (p.Glu585Ala)
ClinVar dbSNP
5g.58975718T=CA1549122008PDE4Dc.1760A= (p.Glu587=)
c.1952A= (p.Glu651=)
c.1622A= (p.Glu541=)
c.1804A= (n.1804A=)
c.1079A= (p.Glu360=)
c.1046A= (p.Glu349=)
c.1544A= (p.Glu515=)
c.1586A= (p.Glu529=)
c.1769A= (p.Glu590=)
c.1562A= (p.Glu521=)
n.1688A=
c.1559A= (p.Glu520=)
c.1280A= (p.Glu427=)
c.1916A= (p.Glu639=)
c.1739A= (p.Glu580=)
c.1532A= (p.Glu511=)
c.1511A= (p.Glu504=)
c.1448A= (p.Glu483=)
c.1184A= (p.Glu395=)
c.1754A= (p.Glu585=)
dbSNP

Number of alleles fetched