| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116783420T>C | CA16602584 | MET | c.*1354T>C (n.*1354T>C) c.3803T>C (p.Met1268Thr) c.3749T>C (p.Met1250Thr) c.2459T>C (p.Met820Thr) c.3806T>C (p.Met1269Thr) n.3880T>C | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.116783420T>A | CA368991889 | MET | c.*1354T>A (n.*1354T>A) c.3803T>A (p.Met1268Lys) c.3749T>A (p.Met1250Lys) c.2459T>A (p.Met820Lys) c.3806T>A (p.Met1269Lys) n.3880T>A | dbSNP |
| 7 | g.116783420T>G | CA368991891 | MET | c.*1354T>G (n.*1354T>G) c.3803T>G (p.Met1268Arg) c.3749T>G (p.Met1250Arg) c.2459T>G (p.Met820Arg) c.3806T>G (p.Met1269Arg) n.3880T>G | dbSNP |