Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.43120184C>TCA009027RETc.2315C>T (p.Ser772Phe)
n.2285C>T
n.2276C>T
c.2711C>T (p.Ser904Phe)
c.*1305C>T (n.*1305C>T)
c.*60C>T (n.*60C>T)
c.1949C>T (p.Ser650Phe)
ClinVar dbSNP gnomAD v4 COSMIC
10g.43120184C>GCA009020RETc.2315C>G (p.Ser772Cys)
n.2285C>G
n.2276C>G
c.2711C>G (p.Ser904Cys)
c.*1305C>G (n.*1305C>G)
c.*60C>G (n.*60C>G)
c.1949C>G (p.Ser650Cys)
ClinVar dbSNP gnomAD v4

Number of alleles fetched