P97S (p.Pro97Ser) variant of EZH2 (Q15910)
P97S (p.Pro97Ser) in EZH2 (Q15910) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data and structural context.
P97S (p.Pro97Ser) variant details
- p.Pro97Ser
- cosmic curated COSV10582
- TOPMed rs1228980656
- gnomAD rs1228980656
- Missense
- Variant Prioritization Score for Impact Estimate 0.674
- REVEL 0.61
- CADD 23.40
- PolyPhen-2 1.00
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available