Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.42323024C>ACA235970STAT3c.1868G>T (p.Trp623Leu)
c.*260G>T (n.*260G>T)
c.1841G>T (p.Trp614Leu)
n.1321G>T
c.*256G>T (n.*256G>T)
c.1964G>T (p.Trp655Leu)
n.2068G>T
c.1847G>T (p.Trp616Leu)
c.1784G>T (p.Trp595Leu)
c.1883G>T (p.Trp628Leu)
n.2305G>T
c.1772G>T (p.Trp591Leu)
n.2285G>T
n.2111G>T
c.1574G>T (p.Trp525Leu)
c.1790G>T (p.Trp597Leu)
c.1808G>T (p.Trp603Leu)
ClinVar dbSNP
17g.42323024C=CA2260430973STAT3c.1868G= (p.Trp623=)
c.*260G= (n.*260G=)
c.1841G= (p.Trp614=)
n.1321G=
c.*256G= (n.*256G=)
c.1964G= (p.Trp655=)
n.2068G=
c.1847G= (p.Trp616=)
c.1784G= (p.Trp595=)
c.1883G= (p.Trp628=)
n.2305G=
c.1772G= (p.Trp591=)
n.2285G=
n.2111G=
c.1574G= (p.Trp525=)
c.1790G= (p.Trp597=)
c.1808G= (p.Trp603=)
dbSNP

Number of alleles fetched