Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.11124517A>TCA16602892MTORc.*2018T>A (n.*2018T>A)
n.2644T>A
c.1280T>A
c.6430T>A (p.Ser2144Thr)
c.*2160T>A (n.*2160T>A)
c.*3473T>A (n.*3473T>A)
c.6643T>A (p.Ser2215Thr)
c.1258T>A (p.Ser420Thr)
n.6764T>A
c.5962T>A (p.Ser1988Thr)
c.5395T>A (p.Ser1799Thr)
ClinVar dbSNP
1g.11124517A>GCA338387279MTORc.*2018T>C (n.*2018T>C)
n.2644T>C
c.1280T>C
c.6430T>C (p.Ser2144Pro)
c.*2160T>C (n.*2160T>C)
c.*3473T>C (n.*3473T>C)
c.6643T>C (p.Ser2215Pro)
c.1258T>C (p.Ser420Pro)
n.6764T>C
c.5962T>C (p.Ser1988Pro)
c.5395T>C (p.Ser1799Pro)
ClinVar dbSNP COSMIC

Number of alleles fetched