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
10g.43120184C>ACA376557281RETc.2315C>A (p.Ser772Tyr)
n.2285C>A
n.2276C>A
c.2711C>A (p.Ser904Tyr)
c.*1305C>A (n.*1305C>A)
c.*60C>A (n.*60C>A)
c.1949C>A (p.Ser650Tyr)
dbSNP COSMIC COSMIC
10g.43120184C=CA1905820005RETc.2315C= (p.Ser772=)
n.2285C=
n.2276C=
c.2711C= (p.Ser904=)
c.*1305C= (n.*1305C=)
c.*60C= (n.*60C=)
c.1949C= (p.Ser650=)
dbSNP

Number of alleles fetched