Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.11114326A>GCA16603392MTORc.*2667T>C (n.*2667T>C)
n.3210T>C
c.2080T>C
c.7079T>C (p.Leu2360Pro)
c.*2809T>C (n.*2809T>C)
c.*4122T>C (n.*4122T>C)
c.7292T>C (p.Leu2431Pro)
c.1907T>C (p.Leu636Pro)
c.260T>C (p.Leu87Pro)
n.304T>C
n.335T>C
n.7330T>C
c.6611T>C (p.Leu2204Pro)
c.6044T>C (p.Leu2015Pro)
ClinVar dbSNP COSMIC
1g.11114326A>TCA338380716MTORc.*2667T>A (n.*2667T>A)
n.3210T>A
c.2080T>A
c.7079T>A (p.Leu2360Gln)
c.*2809T>A (n.*2809T>A)
c.*4122T>A (n.*4122T>A)
c.7292T>A (p.Leu2431Gln)
c.1907T>A (p.Leu636Gln)
c.260T>A (p.Leu87Gln)
n.304T>A
n.335T>A
n.7330T>A
c.6611T>A (p.Leu2204Gln)
c.6044T>A (p.Leu2015Gln)
dbSNP

Number of alleles fetched