Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.11157255A>CCA338372045MTORc.4366T>G (p.Trp1456Gly)
n.286T>G
c.4153T>G (p.Trp1385Gly)
c.*1196T>G (n.*1196T>G)
n.4487T>G
c.3685T>G (p.Trp1229Gly)
c.3118T>G (p.Trp1040Gly)
ClinVar dbSNP
1g.11157255A>TCA338372049MTORc.4366T>A (p.Trp1456Arg)
n.286T>A
c.4153T>A (p.Trp1385Arg)
c.*1196T>A (n.*1196T>A)
n.4487T>A
c.3685T>A (p.Trp1229Arg)
c.3118T>A (p.Trp1040Arg)
dbSNP
1g.11157255A>GCA338372048MTORc.4366T>C (p.Trp1456Arg)
n.286T>C
c.4153T>C (p.Trp1385Arg)
c.*1196T>C (n.*1196T>C)
n.4487T>C
c.3685T>C (p.Trp1229Arg)
c.3118T>C (p.Trp1040Arg)
dbSNP
1g.11157255A=CA1153537952MTORc.4366T= (p.Trp1456=)
n.286T=
c.4153T= (p.Trp1385=)
c.*1196T= (n.*1196T=)
n.4487T=
c.3685T= (p.Trp1229=)
c.3118T= (p.Trp1040=)
dbSNP

Number of alleles fetched