Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.144390001delCA16610153ZEB2c.*2944del (n.*2944del)
c.2318del (p.Cys773LeufsTer?)
c.3095del (p.Cys1032LeufsTer?)
n.3064del
c.2759del (p.Cys920LeufsTer?)
c.3170del (p.Cys1057LeufsTer?)
c.*2812del (n.*2812del)
n.3195del
c.151+6411del (n.151+6411del)
c.315del (n.315del)
c.626del (p.Cys209LeufsTer?)
c.3092del (p.Cys1031LeufsTer?)
c.656-1119del (n.656-1119del)
c.3023del (p.Cys1008LeufsTer?)
c.3086del (p.Cys1029LeufsTer?)
c.3074del (p.Cys1025LeufsTer?)
ClinVar dbSNP
2g.144390001C=CA3085915256ZEB2c.*2944G= (n.*2944G=)
c.2318G= (p.Cys773=)
c.3095G= (p.Cys1032=)
n.3064G=
c.2759G= (p.Cys920=)
c.3170G= (p.Cys1057=)
c.*2812G= (n.*2812G=)
n.3195G=
c.151+6411G= (n.151+6411G=)
c.315G= (n.315G=)
c.626G= (p.Cys209=)
c.3092G= (p.Cys1031=)
c.656-1119G= (n.656-1119G=)
c.3023G= (p.Cys1008=)
c.3086G= (p.Cys1029=)
c.3074G= (p.Cys1025=)
dbSNP

Number of alleles fetched