Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150951097C>GCA006120KCNH2c.1969G>C (p.Gly657Arg)
c.949G>C (p.Gly317Arg)
c.1669G>C (p.Gly557Arg)
c.1819G>C (p.Gly607Arg)
c.1792G>C (p.Gly598Arg)
c.1621G>C (p.Gly541Arg)
n.1256G>C
n.1601G>C
n.2192G>C
ClinVar dbSNP
7g.150951097C>TCA006114KCNH2c.1969G>A (p.Gly657Ser)
c.949G>A (p.Gly317Ser)
c.1669G>A (p.Gly557Ser)
c.1819G>A (p.Gly607Ser)
c.1792G>A (p.Gly598Ser)
c.1621G>A (p.Gly541Ser)
n.1256G>A
n.1601G>A
n.2192G>A
ClinVar dbSNP COSMIC COSMIC COSMIC
7g.150951097C>ACA006126KCNH2c.1969G>T (p.Gly657Cys)
c.949G>T (p.Gly317Cys)
c.1669G>T (p.Gly557Cys)
c.1819G>T (p.Gly607Cys)
c.1792G>T (p.Gly598Cys)
c.1621G>T (p.Gly541Cys)
n.1256G>T
n.1601G>T
n.2192G>T
ClinVar dbSNP

Number of alleles fetched