| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116782027G>T | CA256994 | MET | c.*1167G>T (n.*1167G>T) c.3616G>T (p.Val1206Leu) c.3562G>T (p.Val1188Leu) c.2272G>T (p.Val758Leu) c.3619G>T (p.Val1207Leu) n.3693G>T | ClinVar dbSNP COSMIC |
| 7 | g.116782027G>A | CA4448748 | MET | c.*1167G>A (n.*1167G>A) c.3616G>A (p.Val1206Ile) c.3562G>A (p.Val1188Ile) c.2272G>A (p.Val758Ile) c.3619G>A (p.Val1207Ile) n.3693G>A | ClinVar dbSNP ExAC gnomAD v2 |
| 7 | g.116782027G>C | CA368990990 | MET | c.*1167G>C (n.*1167G>C) c.3616G>C (p.Val1206Leu) c.3562G>C (p.Val1188Leu) c.2272G>C (p.Val758Leu) c.3619G>C (p.Val1207Leu) n.3693G>C | dbSNP COSMIC |
| 7 | g.116782027G= | CA1737012249 | MET | c.*1167G= (n.*1167G=) c.3616G= (p.Val1206=) c.3562G= (p.Val1188=) c.2272G= (p.Val758=) c.3619G= (p.Val1207=) n.3693G= | dbSNP |