Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.15946053C>T | CA16603806 | MYCN | n.700C>T c.1351C>T (p.Gln451Ter) c.718C>T (p.Gln240Ter) c.*1286C>T (n.*1286C>T) | ClinVar dbSNP |
2 | g.15946053C>G | CA345932828 | MYCN | n.700C>G c.1351C>G (p.Gln451Glu) c.718C>G (p.Gln240Glu) c.*1286C>G (n.*1286C>G) | dbSNP COSMIC |