Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.55269880G>CCA16620715TCF4c.873C>G (p.Tyr291Ter)
c.393C>G (p.Tyr131Ter)
n.553C>G
c.801C>G (p.Tyr267Ter)
c.*581C>G (n.*581C>G)
c.483C>G (p.Tyr161Ter)
c.*763C>G (n.*763C>G)
c.225C>G (p.Tyr75Ter)
n.940C>G
n.567C>G
c.471C>G
c.903C>G (p.Tyr301Ter)
c.*484C>G (n.*484C>G)
c.1179C>G (p.Tyr393Ter)
c.747C>G (p.Tyr249Ter)
c.660C>G (p.Tyr220Ter)
n.964C>G
n.728C>G
n.465C>G
c.891C>G (p.Tyr297Ter)
c.621C>G (p.Tyr207Ter)
c.693C>G (p.Tyr231Ter)
c.867C>G (p.Tyr289Ter)
c.834C>G (p.Tyr278Ter)
c.798C>G (p.Tyr266Ter)
c.137C>G
n.733C>G
n.524-8347C>G
c.*16C>G (n.*16C>G)
c.663C>G (p.Tyr221Ter)
c.870C>G (p.Tyr290Ter)
c.1176C>G (p.Tyr392Ter)
c.636C>G (p.Tyr212Ter)
ClinVar dbSNP
18g.55269880G=CA2305022649TCF4c.873C= (p.Tyr291=)
c.393C= (p.Tyr131=)
n.553C=
c.801C= (p.Tyr267=)
c.*581C= (n.*581C=)
c.483C= (p.Tyr161=)
c.*763C= (n.*763C=)
c.225C= (p.Tyr75=)
n.940C=
n.567C=
c.471C=
c.903C= (p.Tyr301=)
c.*484C= (n.*484C=)
c.1179C= (p.Tyr393=)
c.747C= (p.Tyr249=)
c.660C= (p.Tyr220=)
n.964C=
n.728C=
n.465C=
c.891C= (p.Tyr297=)
c.621C= (p.Tyr207=)
c.693C= (p.Tyr231=)
c.867C= (p.Tyr289=)
c.834C= (p.Tyr278=)
c.798C= (p.Tyr266=)
c.137C=
n.733C=
n.524-8347C=
c.*16C= (n.*16C=)
c.663C= (p.Tyr221=)
c.870C= (p.Tyr290=)
c.1176C= (p.Tyr392=)
c.636C= (p.Tyr212=)
dbSNP

Number of alleles fetched