Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.42323046C>TCA399582847STAT3c.1846G>A (p.Glu616Lys)
c.*238G>A (n.*238G>A)
c.1819G>A (p.Glu607Lys)
n.1299G>A
c.*234G>A (n.*234G>A)
c.1942G>A (p.Glu648Lys)
n.2046G>A
c.1825G>A (p.Glu609Lys)
c.1762G>A (p.Glu588Lys)
c.1861G>A (p.Glu621Lys)
n.2283G>A
c.1750G>A (p.Glu584Lys)
n.2263G>A
n.2089G>A
c.1552G>A (p.Glu518Lys)
n.815G>A
c.1768G>A (p.Glu590Lys)
c.1786G>A (p.Glu596Lys)
dbSNP COSMIC
17g.42323046C>ACA399582844STAT3c.1846G>T (p.Glu616Ter)
c.*238G>T (n.*238G>T)
c.1819G>T (p.Glu607Ter)
n.1299G>T
c.*234G>T (n.*234G>T)
c.1942G>T (p.Glu648Ter)
n.2046G>T
c.1825G>T (p.Glu609Ter)
c.1762G>T (p.Glu588Ter)
c.1861G>T (p.Glu621Ter)
n.2283G>T
c.1750G>T (p.Glu584Ter)
n.2263G>T
n.2089G>T
c.1552G>T (p.Glu518Ter)
n.815G>T
c.1768G>T (p.Glu590Ter)
c.1786G>T (p.Glu596Ter)
dbSNP
17g.42323046C>GCA16620411STAT3c.1846G>C (p.Glu616Gln)
c.*238G>C (n.*238G>C)
c.1819G>C (p.Glu607Gln)
n.1299G>C
c.*234G>C (n.*234G>C)
c.1942G>C (p.Glu648Gln)
n.2046G>C
c.1825G>C (p.Glu609Gln)
c.1762G>C (p.Glu588Gln)
c.1861G>C (p.Glu621Gln)
n.2283G>C
c.1750G>C (p.Glu584Gln)
n.2263G>C
n.2089G>C
c.1552G>C (p.Glu518Gln)
n.815G>C
c.1768G>C (p.Glu590Gln)
c.1786G>C (p.Glu596Gln)
ClinVar dbSNP

Number of alleles fetched