| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.17085639T>C | CA144259 | CUBN | c.2068A>G (p.Ile690Val) | ClinVar dbSNP |
| 10 | g.17085639T>A | CA376149469 | CUBN | c.2068A>T (p.Ile690Phe) | dbSNP gnomAD v4 |
| 10 | g.17085639T= | CA1893460194 | CUBN | c.2068A= (p.Ile690=) | dbSNP |