Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.47566722C>GCA16602595ARAFc.641C>G (p.Ser214Cys)
c.650C>G (p.Ser217Cys)
c.656C>G (p.Ser219Cys)
c.-17C>G (n.-17C>G)
ClinVar dbSNP COSMIC
Xg.47566722C>ACA412813393ARAFc.641C>A (p.Ser214Tyr)
c.650C>A (p.Ser217Tyr)
c.656C>A (p.Ser219Tyr)
c.-17C>A (n.-17C>A)
dbSNP COSMIC
Xg.47566722C>TCA16602805ARAFc.641C>T (p.Ser214Phe)
c.650C>T (p.Ser217Phe)
c.656C>T (p.Ser219Phe)
c.-17C>T (n.-17C>T)
ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched