| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116777427A>T | CA16603137 | MET | c.*903A>T (n.*903A>T) c.3352A>T (p.Asn1118Tyr) c.3298A>T (p.Asn1100Tyr) c.2008A>T (p.Asn670Tyr) c.3355A>T (p.Asn1119Tyr) n.3429A>T | ClinVar dbSNP COSMIC |
| 7 | g.116777427A>G | CA368989664 | MET | c.*903A>G (n.*903A>G) c.3352A>G (p.Asn1118Asp) c.3298A>G (p.Asn1100Asp) c.2008A>G (p.Asn670Asp) c.3355A>G (p.Asn1119Asp) n.3429A>G | dbSNP gnomAD v2 COSMIC |