| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116783329G>A | CA256997 | MET | c.*1263G>A (n.*1263G>A) c.3712G>A (p.Val1238Ile) c.3658G>A (p.Val1220Ile) c.2368G>A (p.Val790Ile) c.3715G>A (p.Val1239Ile) n.3789G>A | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.116783329G>T | CA368991472 | MET | c.*1263G>T (n.*1263G>T) c.3712G>T (p.Val1238Phe) c.3658G>T (p.Val1220Phe) c.2368G>T (p.Val790Phe) c.3715G>T (p.Val1239Phe) n.3789G>T | ClinVar dbSNP |
| 7 | g.116783329G>C | CA368991469 | MET | c.*1263G>C (n.*1263G>C) c.3712G>C (p.Val1238Leu) c.3658G>C (p.Val1220Leu) c.2368G>C (p.Val790Leu) c.3715G>C (p.Val1239Leu) n.3789G>C | ClinVar dbSNP |