Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47799259delCA008430FBXO11,MSH6c.979del (p.Cys327ValfsTer27)
c.1276del (p.Cys426ValfsTer27)
n.1360del
c.1282del (p.Cys428ValfsTer27)
c.627+3196del (n.627+3196del)
c.433del (p.Cys145ValfsTer27)
c.886del (p.Cys296ValfsTer27)
c.169+8936del (n.169+8936del)
c.*124+8735del (n.*124+8735del)
c.*623del (n.*623del)
c.370del (p.Cys124ValfsTer27)
c.1273del (p.Cys425ValfsTer27)
c.-1821del (n.-1821del)
c.1093del (p.Cys365ValfsTer27)
ClinVar dbSNP
2g.47799259T=CA3085660856FBXO11,MSH6c.979T= (p.Cys327=)
c.1276T= (p.Cys426=)
n.1360T=
c.1282T= (p.Cys428=)
c.627+3196T= (n.627+3196T=)
c.433T= (p.Cys145=)
c.886T= (p.Cys296=)
c.169+8936A= (n.169+8936A=)
c.*124+8735A= (n.*124+8735A=)
c.*623T= (n.*623T=)
c.370T= (p.Cys124=)
c.1273T= (p.Cys425=)
c.-1821T= (n.-1821T=)
c.1093T= (p.Cys365=)
dbSNP dbSNP dbSNP

Number of alleles fetched