Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.13257474A>GCA254443CACNA1Ac.4466T>C (p.Phe1489Ser)
c.4472T>C (p.Phe1491Ser)
c.4469T>C (p.Phe1490Ser)
n.455T>C
n.958T>C
n.1154T>C
n.749T>C
n.932T>C
n.1693T>C
c.122T>C (p.Phe41Ser)
c.4478T>C (p.Phe1493Ser)
n.788T>C
c.4328T>C (p.Phe1443Ser)
c.4664T>C (p.Phe1555Ser)
c.524T>C (p.Phe175Ser)
ClinVar dbSNP
19g.13257474A>TCA404339002CACNA1Ac.4466T>A (p.Phe1489Tyr)
c.4472T>A (p.Phe1491Tyr)
c.4469T>A (p.Phe1490Tyr)
n.455T>A
n.958T>A
n.1154T>A
n.749T>A
n.932T>A
n.1693T>A
c.122T>A (p.Phe41Tyr)
c.4478T>A (p.Phe1493Tyr)
n.788T>A
c.4328T>A (p.Phe1443Tyr)
c.4664T>A (p.Phe1555Tyr)
c.524T>A (p.Phe175Tyr)
dbSNP
19g.13257474A=CA2323806445CACNA1Ac.4466T= (p.Phe1489=)
c.4472T= (p.Phe1491=)
c.4469T= (p.Phe1490=)
n.455T=
n.958T=
n.1154T=
n.749T=
n.932T=
n.1693T=
c.122T= (p.Phe41=)
c.4478T= (p.Phe1493=)
n.788T=
c.4328T= (p.Phe1443=)
c.4664T= (p.Phe1555=)
c.524T= (p.Phe175=)
dbSNP

Number of alleles fetched