Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.11114338A>CCA338380764MTORc.*2655T>G (n.*2655T>G)
n.3198T>G
c.2068T>G
c.7067T>G (p.Leu2356Arg)
c.*2797T>G (n.*2797T>G)
c.*4110T>G (n.*4110T>G)
c.7280T>G (p.Leu2427Arg)
c.1895T>G (p.Leu632Arg)
c.248T>G (p.Leu83Arg)
n.292T>G
n.323T>G
n.7318T>G
c.6599T>G (p.Leu2200Arg)
c.6032T>G (p.Leu2011Arg)
dbSNP COSMIC
1g.11114338A>GCA338380762MTORc.*2655T>C (n.*2655T>C)
n.3198T>C
c.2068T>C
c.7067T>C (p.Leu2356Pro)
c.*2797T>C (n.*2797T>C)
c.*4110T>C (n.*4110T>C)
c.7280T>C (p.Leu2427Pro)
c.1895T>C (p.Leu632Pro)
c.248T>C (p.Leu83Pro)
n.292T>C
n.323T>C
n.7318T>C
c.6599T>C (p.Leu2200Pro)
c.6032T>C (p.Leu2011Pro)
ClinVar dbSNP COSMIC
1g.11114338A>TCA338380760MTORc.*2655T>A (n.*2655T>A)
n.3198T>A
c.2068T>A
c.7067T>A (p.Leu2356Gln)
c.*2797T>A (n.*2797T>A)
c.*4110T>A (n.*4110T>A)
c.7280T>A (p.Leu2427Gln)
c.1895T>A (p.Leu632Gln)
c.248T>A (p.Leu83Gln)
n.292T>A
n.323T>A
n.7318T>A
c.6599T>A (p.Leu2200Gln)
c.6032T>A (p.Leu2011Gln)
ClinVar dbSNP COSMIC

Number of alleles fetched