| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116783374T>A | CA368991657 | MET | c.*1308T>A (n.*1308T>A) c.3757T>A (p.Tyr1253Asn) c.3703T>A (p.Tyr1235Asn) c.2413T>A (p.Tyr805Asn) c.3760T>A (p.Tyr1254Asn) n.3834T>A | dbSNP |
| 7 | g.116783374T>C | CA368991658 | MET | c.*1308T>C (n.*1308T>C) c.3757T>C (p.Tyr1253His) c.3703T>C (p.Tyr1235His) c.2413T>C (p.Tyr805His) c.3760T>C (p.Tyr1254His) n.3834T>C | dbSNP COSMIC |
| 7 | g.116783374T>G | CA16602655 | MET | c.*1308T>G (n.*1308T>G) c.3757T>G (p.Tyr1253Asp) c.3703T>G (p.Tyr1235Asp) c.2413T>G (p.Tyr805Asp) c.3760T>G (p.Tyr1254Asp) n.3834T>G | ClinVar dbSNP COSMIC |