| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.102550088C>T | CA16612979 | SUFU | c.436C>T (p.Arg146Ter) c.358C>T (p.Arg120Ter) c.262C>T (p.Arg88Ter) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.102550088C= | CA1932722482 | SUFU | c.436C= (p.Arg146=) c.358C= (p.Arg120=) c.262C= (p.Arg88=) | dbSNP |