Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.29222404A>T | CA346463324 | ALK | c.3455T>A (p.Leu1152Gln) c.682T>A n.332T>A c.251T>A (p.Leu84Gln) c.335T>A (p.Leu112Gln) c.149T>A (p.Leu50Gln) c.2324T>A (p.Leu775Gln) c.608T>A (p.Leu203Gln) | dbSNP |
2 | g.29222404A>C | CA16602594 | ALK | c.3455T>G (p.Leu1152Arg) c.682T>G n.332T>G c.251T>G (p.Leu84Arg) c.335T>G (p.Leu112Arg) c.149T>G (p.Leu50Arg) c.2324T>G (p.Leu775Arg) c.608T>G (p.Leu203Arg) | ClinVar dbSNP COSMIC |
2 | g.29222404A>G | CA346463323 | ALK | c.3455T>C (p.Leu1152Pro) c.682T>C n.332T>C c.251T>C (p.Leu84Pro) c.335T>C (p.Leu112Pro) c.149T>C (p.Leu50Pro) c.2324T>C (p.Leu775Pro) c.608T>C (p.Leu203Pro) | dbSNP |