Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.11157173C>TCA16602888MTORc.4448G>A (p.Cys1483Tyr)
n.368G>A
c.4235G>A (p.Cys1412Tyr)
c.*1278G>A (n.*1278G>A)
n.4569G>A
c.3767G>A (p.Cys1256Tyr)
c.3200G>A (p.Cys1067Tyr)
ClinVar dbSNP COSMIC
1g.11157173C>ACA199563MTORc.4448G>T (p.Cys1483Phe)
n.368G>T
c.4235G>T (p.Cys1412Phe)
c.*1278G>T (n.*1278G>T)
n.4569G>T
c.3767G>T (p.Cys1256Phe)
c.3200G>T (p.Cys1067Phe)
ClinVar dbSNP COSMIC
1g.11157173C>GCA338371562MTORc.4448G>C (p.Cys1483Ser)
n.368G>C
c.4235G>C (p.Cys1412Ser)
c.*1278G>C (n.*1278G>C)
n.4569G>C
c.3767G>C (p.Cys1256Ser)
c.3200G>C (p.Cys1067Ser)
dbSNP

Number of alleles fetched