Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.42322440A>TCA16620410STAT3c.1943T>A (p.Met648Lys)
c.*335T>A (n.*335T>A)
c.1916T>A (p.Met639Lys)
n.1396T>A
c.*331T>A (n.*331T>A)
c.2039T>A (p.Met680Lys)
n.2143T>A
c.1922T>A (p.Met641Lys)
c.1859T>A (p.Met620Lys)
c.1958T>A (p.Met653Lys)
n.2380T>A
c.1847T>A (p.Met616Lys)
n.2360T>A
n.2186T>A
c.1649T>A (p.Met550Lys)
c.1865T>A (p.Met622Lys)
c.1883T>A (p.Met628Lys)
ClinVar dbSNP
17g.42322440A=CA2260430742STAT3c.1943T= (p.Met648=)
c.*335T= (n.*335T=)
c.1916T= (p.Met639=)
n.1396T=
c.*331T= (n.*331T=)
c.2039T= (p.Met680=)
n.2143T=
c.1922T= (p.Met641=)
c.1859T= (p.Met620=)
c.1958T= (p.Met653=)
n.2380T=
c.1847T= (p.Met616=)
n.2360T=
n.2186T=
c.1649T= (p.Met550=)
c.1865T= (p.Met622=)
c.1883T= (p.Met628=)
dbSNP
17g.42322440A>GCA399582284STAT3c.1943T>C (p.Met648Thr)
c.*335T>C (n.*335T>C)
c.1916T>C (p.Met639Thr)
n.1396T>C
c.*331T>C (n.*331T>C)
c.2039T>C (p.Met680Thr)
n.2143T>C
c.1922T>C (p.Met641Thr)
c.1859T>C (p.Met620Thr)
c.1958T>C (p.Met653Thr)
n.2380T>C
c.1847T>C (p.Met616Thr)
n.2360T>C
n.2186T>C
c.1649T>C (p.Met550Thr)
c.1865T>C (p.Met622Thr)
c.1883T>C (p.Met628Thr)
ClinVar dbSNP

Number of alleles fetched