Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.136505776A>GCA349407NOTCH1n.1927T>C
c.4120T>C (p.Cys1374Arg)
c.4006T>C (p.Cys1336Arg)
c.4000T>C (p.Cys1334Arg)
c.1717T>C (p.Cys573Arg)
c.*1520T>C (n.*1520T>C)
c.*1729T>C (n.*1729T>C)
n.933T>C
c.*3356T>C (n.*3356T>C)
c.3421T>C (p.Cys1141Arg)
c.3397T>C (p.Cys1133Arg)
ClinVar dbSNP
9g.136505776A>CCA375649680NOTCH1n.1927T>G
c.4120T>G (p.Cys1374Gly)
c.4006T>G (p.Cys1336Gly)
c.4000T>G (p.Cys1334Gly)
c.1717T>G (p.Cys573Gly)
c.*1520T>G (n.*1520T>G)
c.*1729T>G (n.*1729T>G)
n.933T>G
c.*3356T>G (n.*3356T>G)
c.3421T>G (p.Cys1141Gly)
c.3397T>G (p.Cys1133Gly)
dbSNP
9g.136505776A>TCA375649683NOTCH1n.1927T>A
c.4120T>A (p.Cys1374Ser)
c.4006T>A (p.Cys1336Ser)
c.4000T>A (p.Cys1334Ser)
c.1717T>A (p.Cys573Ser)
c.*1520T>A (n.*1520T>A)
c.*1729T>A (n.*1729T>A)
n.933T>A
c.*3356T>A (n.*3356T>A)
c.3421T>A (p.Cys1141Ser)
c.3397T>A (p.Cys1133Ser)
dbSNP
9g.136505776A=CA3165601231NOTCH1n.1927T=
c.4120T= (p.Cys1374=)
c.4006T= (p.Cys1336=)
c.4000T= (p.Cys1334=)
c.1717T= (p.Cys573=)
c.*1520T= (n.*1520T=)
c.*1729T= (n.*1729T=)
n.933T=
c.*3356T= (n.*3356T=)
c.3421T= (p.Cys1141=)
c.3397T= (p.Cys1133=)
dbSNP

Number of alleles fetched