| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.116798111C>T | CA10623079 | MET | c.*3765C>T (n.*3765C>T) c.*1987C>T (n.*1987C>T) n.6291C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.116798111C>A | CA165451231 | MET | c.*3765C>A (n.*3765C>A) c.*1987C>A (n.*1987C>A) n.6291C>A | dbSNP gnomAD v4 |