Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43113649G>TCA008022RETc.1853G>T (p.Cys618Phe)
c.1091G>T (p.Cys364Phe)
c.404G>T (p.Cys135Phe)
c.1289+2417G>T (p.=)
ClinVar dbSNP
10g.43113649G>CCA008013RETc.1853G>C (p.Cys618Ser)
c.1091G>C (p.Cys364Ser)
c.404G>C (p.Cys135Ser)
c.1289+2417G>C (p.=)
ClinVar dbSNP
10g.43113649G>ACA008005RETc.1853G>A (p.Cys618Tyr)
c.1091G>A (p.Cys364Tyr)
c.404G>A (p.Cys135Tyr)
c.1289+2417G>A (p.=)
ClinVar dbSNP COSMIC COSMIC

Number of alleles fetched