Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.144403918G>ACA267217ZEB2c.*654C>T (n.*654C>T)
c.28C>T (p.Gln10Ter)
c.805C>T (p.Gln269Ter)
n.774C>T
c.469C>T (p.Gln157Ter)
c.*522C>T (n.*522C>T)
n.905C>T
c.-133-5068C>T (n.-133-5068C>T)
c.802C>T (p.Gln268Ter)
c.889C>T (p.Gln297Ter)
c.544C>T (p.Gln182Ter)
c.892C>T (p.Gln298Ter)
c.790C>T (p.Gln264Ter)
c.733C>T (p.Gln245Ter)
c.796C>T (p.Gln266Ter)
c.784C>T (p.Gln262Ter)
ClinVar dbSNP
2g.144403918G=CA1294887161ZEB2c.*654C= (n.*654C=)
c.28C= (p.Gln10=)
c.805C= (p.Gln269=)
n.774C=
c.469C= (p.Gln157=)
c.*522C= (n.*522C=)
n.905C=
c.-133-5068C= (n.-133-5068C=)
c.802C= (p.Gln268=)
c.889C= (p.Gln297=)
c.544C= (p.Gln182=)
c.892C= (p.Gln298=)
c.790C= (p.Gln264=)
c.733C= (p.Gln245=)
c.796C= (p.Gln266=)
c.784C= (p.Gln262=)
dbSNP

Number of alleles fetched