| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116783421G>T | CA16602657 | MET | c.*1355G>T (n.*1355G>T) c.3804G>T (p.Met1268Ile) c.3750G>T (p.Met1250Ile) c.2460G>T (p.Met820Ile) c.3807G>T (p.Met1269Ile) n.3881G>T | ClinVar dbSNP |
| 7 | g.116783421G>C | CA16602656 | MET | c.*1355G>C (n.*1355G>C) c.3804G>C (p.Met1268Ile) c.3750G>C (p.Met1250Ile) c.2460G>C (p.Met820Ile) c.3807G>C (p.Met1269Ile) n.3881G>C | ClinVar dbSNP |
| 7 | g.116783421G>A | CA123611 | MET | c.*1355G>A (n.*1355G>A) c.3804G>A (p.Met1268Ile) c.3750G>A (p.Met1250Ile) c.2460G>A (p.Met820Ile) c.3807G>A (p.Met1269Ile) n.3881G>A | ClinVar dbSNP COSMIC |
| 7 | g.116783421G= | CA1737014581 | MET | c.*1355G= (n.*1355G=) c.3804G= (p.Met1268=) c.3750G= (p.Met1250=) c.2460G= (p.Met820=) c.3807G= (p.Met1269=) n.3881G= | dbSNP |