Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.87931078T>ACA377481367PTENc.242T>A (p.Phe81Tyr)
n.977T>A
c.*72T>A (n.*72T>A)
c.197T>A (p.Phe66Tyr)
c.76T>A
c.*277T>A (n.*277T>A)
c.*353T>A (n.*353T>A)
c.163T>A
c.761T>A (p.Phe254Tyr)
n.68T>A
c.140T>A (p.Phe47Tyr)
c.-509T>A (n.-509T>A)
c.146T>A (p.Phe49Tyr)
n.954T>A
ClinVar dbSNP
10g.87931078T>GCA10577417PTENc.242T>G (p.Phe81Cys)
n.977T>G
c.*72T>G (n.*72T>G)
c.197T>G (p.Phe66Cys)
c.76T>G
c.*277T>G (n.*277T>G)
c.*353T>G (n.*353T>G)
c.163T>G
c.761T>G (p.Phe254Cys)
n.68T>G
c.140T>G (p.Phe47Cys)
c.-509T>G (n.-509T>G)
c.146T>G (p.Phe49Cys)
n.954T>G
ClinVar dbSNP COSMIC

Number of alleles fetched