Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.42322413T>GCA399582026STAT3c.1970A>C (p.Tyr657Ser)
c.*362A>C (n.*362A>C)
c.1943A>C (p.Tyr648Ser)
n.1423A>C
c.*358A>C (n.*358A>C)
c.2066A>C (p.Tyr689Ser)
n.2170A>C
c.1949A>C (p.Tyr650Ser)
c.1886A>C (p.Tyr629Ser)
c.1985A>C (p.Tyr662Ser)
n.2407A>C
c.1874A>C (p.Tyr625Ser)
n.2387A>C
n.2213A>C
c.1676A>C (p.Tyr559Ser)
c.1892A>C (p.Tyr631Ser)
c.1910A>C (p.Tyr637Ser)
dbSNP
17g.42322413T>ACA399582030STAT3c.1970A>T (p.Tyr657Phe)
c.*362A>T (n.*362A>T)
c.1943A>T (p.Tyr648Phe)
n.1423A>T
c.*358A>T (n.*358A>T)
c.2066A>T (p.Tyr689Phe)
n.2170A>T
c.1949A>T (p.Tyr650Phe)
c.1886A>T (p.Tyr629Phe)
c.1985A>T (p.Tyr662Phe)
n.2407A>T
c.1874A>T (p.Tyr625Phe)
n.2387A>T
n.2213A>T
c.1676A>T (p.Tyr559Phe)
c.1892A>T (p.Tyr631Phe)
c.1910A>T (p.Tyr637Phe)
dbSNP
17g.42322413T>CCA260546STAT3c.1970A>G (p.Tyr657Cys)
c.*362A>G (n.*362A>G)
c.1943A>G (p.Tyr648Cys)
n.1423A>G
c.*358A>G (n.*358A>G)
c.2066A>G (p.Tyr689Cys)
n.2170A>G
c.1949A>G (p.Tyr650Cys)
c.1886A>G (p.Tyr629Cys)
c.1985A>G (p.Tyr662Cys)
n.2407A>G
c.1874A>G (p.Tyr625Cys)
n.2387A>G
n.2213A>G
c.1676A>G (p.Tyr559Cys)
c.1892A>G (p.Tyr631Cys)
c.1910A>G (p.Tyr637Cys)
ClinVar dbSNP

Number of alleles fetched