Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.42322474C>TCA341510STAT3c.1909G>A (p.Val637Met)
c.*301G>A (n.*301G>A)
c.1882G>A (p.Val628Met)
n.1362G>A
c.*297G>A (n.*297G>A)
c.2005G>A (p.Val669Met)
n.2109G>A
c.1888G>A (p.Val630Met)
c.1825G>A (p.Val609Met)
c.1924G>A (p.Val642Met)
n.2346G>A
c.1813G>A (p.Val605Met)
n.2326G>A
n.2152G>A
c.1615G>A (p.Val539Met)
c.1831G>A (p.Val611Met)
c.1849G>A (p.Val617Met)
ClinVar dbSNP
17g.42322474C>ACA399582495STAT3c.1909G>T (p.Val637Leu)
c.*301G>T (n.*301G>T)
c.1882G>T (p.Val628Leu)
n.1362G>T
c.*297G>T (n.*297G>T)
c.2005G>T (p.Val669Leu)
n.2109G>T
c.1888G>T (p.Val630Leu)
c.1825G>T (p.Val609Leu)
c.1924G>T (p.Val642Leu)
n.2346G>T
c.1813G>T (p.Val605Leu)
n.2326G>T
n.2152G>T
c.1615G>T (p.Val539Leu)
c.1831G>T (p.Val611Leu)
c.1849G>T (p.Val617Leu)
ClinVar dbSNP
17g.42322474C>GCA399582497STAT3c.1909G>C (p.Val637Leu)
c.*301G>C (n.*301G>C)
c.1882G>C (p.Val628Leu)
n.1362G>C
c.*297G>C (n.*297G>C)
c.2005G>C (p.Val669Leu)
n.2109G>C
c.1888G>C (p.Val630Leu)
c.1825G>C (p.Val609Leu)
c.1924G>C (p.Val642Leu)
n.2346G>C
c.1813G>C (p.Val605Leu)
n.2326G>C
n.2152G>C
c.1615G>C (p.Val539Leu)
c.1831G>C (p.Val611Leu)
c.1849G>C (p.Val617Leu)
dbSNP

Number of alleles fetched