Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.144389962T>CCA264211ZEB2c.*2983A>G (n.*2983A>G)
c.2357A>G (p.His786Arg)
c.3134A>G (p.His1045Arg)
n.3103A>G
c.2798A>G (p.His933Arg)
c.3209A>G (p.His1070Arg)
c.*2851A>G (n.*2851A>G)
n.3234A>G
c.151+6450A>G (n.151+6450A>G)
c.354A>G (n.354A>G)
c.665A>G (p.His222Arg)
c.3131A>G (p.His1044Arg)
c.656-1080A>G (n.656-1080A>G)
c.3062A>G (p.His1021Arg)
c.3125A>G (p.His1042Arg)
c.3113A>G (p.His1038Arg)
ClinVar dbSNP
2g.144389962T>ACA348701058ZEB2c.*2983A>T (n.*2983A>T)
c.2357A>T (p.His786Leu)
c.3134A>T (p.His1045Leu)
n.3103A>T
c.2798A>T (p.His933Leu)
c.3209A>T (p.His1070Leu)
c.*2851A>T (n.*2851A>T)
n.3234A>T
c.151+6450A>T (n.151+6450A>T)
c.354A>T (n.354A>T)
c.665A>T (p.His222Leu)
c.3131A>T (p.His1044Leu)
c.656-1080A>T (n.656-1080A>T)
c.3062A>T (p.His1021Leu)
c.3125A>T (p.His1042Leu)
c.3113A>T (p.His1038Leu)
ClinVar dbSNP
2g.144389962T=CA1294881399ZEB2c.*2983A= (n.*2983A=)
c.2357A= (p.His786=)
c.3134A= (p.His1045=)
n.3103A=
c.2798A= (p.His933=)
c.3209A= (p.His1070=)
c.*2851A= (n.*2851A=)
n.3234A=
c.151+6450A= (n.151+6450A=)
c.354A= (n.354A=)
c.665A= (p.His222=)
c.3131A= (p.His1044=)
c.656-1080A= (n.656-1080A=)
c.3062A= (p.His1021=)
c.3125A= (p.His1042=)
c.3113A= (p.His1038=)
dbSNP

Number of alleles fetched