| Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
| PPP3CB | 9315 | COSM5009175, | large_intestine | carcinoma | p.R341Q | Substitution - Missense | 10:73467639-73467639, | PATHOGENIC | 0.98199 | 24951259 |
| PPP3CB | 9315 | COSM5009178, | large_intestine | carcinoma | p.E68E | Substitution - coding silent | 10:73479399-73479399, | PATHOGENIC | 0.86904 | 24951259 |