Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.15946053C>TCA16603806MYCNn.700C>T
c.1351C>T (p.Gln451Ter)
c.718C>T (p.Gln240Ter)
c.*1286C>T (n.*1286C>T)
ClinVar dbSNP
2g.15946053C>GCA345932828MYCNn.700C>G
c.1351C>G (p.Gln451Glu)
c.718C>G (p.Gln240Glu)
c.*1286C>G (n.*1286C>G)
dbSNP COSMIC

Number of alleles fetched