Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.55259981G>CCA16043152TCF4c.1037C>G (p.Ser346Ter)
c.557C>G (p.Ser186Ter)
n.717C>G
c.965C>G (p.Ser322Ter)
c.*745C>G (n.*745C>G)
c.647C>G (p.Ser216Ter)
c.*927C>G (n.*927C>G)
c.389C>G (p.Ser130Ter)
n.1104C>G
n.731C>G
c.635C>G
c.1067C>G (p.Ser356Ter)
c.*648C>G (n.*648C>G)
c.1343C>G (p.Ser448Ter)
c.911C>G (p.Ser304Ter)
c.824C>G (p.Ser275Ter)
n.1128C>G
n.582+1485C>G
c.1055C>G (p.Ser352Ter)
c.785C>G (p.Ser262Ter)
c.857C>G (p.Ser286Ter)
c.1031C>G (p.Ser344Ter)
c.962C>G (p.Ser321Ter)
c.301C>G
c.*180C>G (n.*180C>G)
c.1034C>G (p.Ser345Ter)
c.827C>G (p.Ser276Ter)
c.1340C>G (p.Ser447Ter)
c.800C>G (p.Ser267Ter)
ClinVar dbSNP
18g.55259981G=CA2305018479TCF4c.1037C= (p.Ser346=)
c.557C= (p.Ser186=)
n.717C=
c.965C= (p.Ser322=)
c.*745C= (n.*745C=)
c.647C= (p.Ser216=)
c.*927C= (n.*927C=)
c.389C= (p.Ser130=)
n.1104C=
n.731C=
c.635C=
c.1067C= (p.Ser356=)
c.*648C= (n.*648C=)
c.1343C= (p.Ser448=)
c.911C= (p.Ser304=)
c.824C= (p.Ser275=)
n.1128C=
n.582+1485C=
c.1055C= (p.Ser352=)
c.785C= (p.Ser262=)
c.857C= (p.Ser286=)
c.1031C= (p.Ser344=)
c.962C= (p.Ser321=)
c.301C=
c.*180C= (n.*180C=)
c.1034C= (p.Ser345=)
c.827C= (p.Ser276=)
c.1340C= (p.Ser447=)
c.800C= (p.Ser267=)
dbSNP

Number of alleles fetched