| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116778953C>T | CA123608 | MET | c.*1123C>T (n.*1123C>T) c.3572C>T (p.Thr1191Ile) c.3518C>T (p.Thr1173Ile) c.2228C>T (p.Thr743Ile) c.3575C>T (p.Thr1192Ile) n.3649C>T | ClinVar dbSNP COSMIC |
| 7 | g.116778953C>A | CA368990386 | MET | c.*1123C>A (n.*1123C>A) c.3572C>A (p.Thr1191Asn) c.3518C>A (p.Thr1173Asn) c.2228C>A (p.Thr743Asn) c.3575C>A (p.Thr1192Asn) n.3649C>A | dbSNP |
| 7 | g.116778953C>G | CA368990385 | MET | c.*1123C>G (n.*1123C>G) c.3572C>G (p.Thr1191Ser) c.3518C>G (p.Thr1173Ser) c.2228C>G (p.Thr743Ser) c.3575C>G (p.Thr1192Ser) n.3649C>G | ClinVar dbSNP |