Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.11117039C>ACA338383476MTORc.*2356G>T (n.*2356G>T)
n.2935-1571G>T
c.1769G>T
c.6768G>T (p.Met2256Ile)
c.*2498G>T (n.*2498G>T)
c.*3811G>T (n.*3811G>T)
c.6981G>T (p.Met2327Ile)
c.1596G>T (p.Met532Ile)
n.7055-1571G>T
c.6300G>T (p.Met2100Ile)
c.5733G>T (p.Met1911Ile)
dbSNP COSMIC
1g.11117039C>TCA10583991MTORc.*2356G>A (n.*2356G>A)
n.2935-1571G>A
c.1769G>A
c.6768G>A (p.Met2256Ile)
c.*2498G>A (n.*2498G>A)
c.*3811G>A (n.*3811G>A)
c.6981G>A (p.Met2327Ile)
c.1596G>A (p.Met532Ile)
n.7055-1571G>A
c.6300G>A (p.Met2100Ile)
c.5733G>A (p.Met1911Ile)
ClinVar dbSNP COSMIC

Number of alleles fetched