| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116777403G>C | CA368989570 | MET | c.*879G>C (n.*879G>C) c.3328G>C (p.Val1110Leu) c.3274G>C (p.Val1092Leu) c.1984G>C (p.Val662Leu) c.3331G>C (p.Val1111Leu) n.3405G>C | dbSNP |
| 7 | g.116777403G>A | CA193972 | MET | c.*879G>A (n.*879G>A) c.3328G>A (p.Val1110Ile) c.3274G>A (p.Val1092Ile) c.1984G>A (p.Val662Ile) c.3331G>A (p.Val1111Ile) n.3405G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.116777403G= | CA1737039884 | MET | c.*879G= (n.*879G=) c.3328G= (p.Val1110=) c.3274G= (p.Val1092=) c.1984G= (p.Val662=) c.3331G= (p.Val1111=) n.3405G= | dbSNP |
| 7 | g.116777403G>T | CA368989572 | MET | c.*879G>T (n.*879G>T) c.3328G>T (p.Val1110Leu) c.3274G>T (p.Val1092Leu) c.1984G>T (p.Val662Leu) c.3331G>T (p.Val1111Leu) n.3405G>T | ClinVar dbSNP |