Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43113654T>GCA008066RETc.1858T>G (p.Cys620Gly)
c.1096T>G (p.Cys366Gly)
c.409T>G (p.Cys137Gly)
c.1289+2422T>G (p.=)
ClinVar dbSNP
10g.43113654T>CCA008055RETc.1858T>C (p.Cys620Arg)
c.1096T>C (p.Cys366Arg)
c.409T>C (p.Cys137Arg)
c.1289+2422T>C (p.=)
ClinVar dbSNP COSMIC
10g.43113654T>ACA008047RETc.1858T>A (p.Cys620Ser)
c.1096T>A (p.Cys366Ser)
c.409T>A (p.Cys137Ser)
c.1289+2422T>A (p.=)
ClinVar dbSNP COSMIC

Number of alleles fetched