| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.17068723G>T | CA144271 | CUBN | c.2673C>A (p.Cys891Ter) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.17068723G>C | CA5424901 | CUBN | c.2673C>G (p.Cys891Trp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.17068723G>A | CA5424902 | CUBN | c.2673C>T (p.Cys891=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |