P66Q (p.Pro66Gln) variant of MCL1 (Q07820)
P66Q (p.Pro66Gln) in MCL1 (Q07820) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
P66Q (p.Pro66Gln) variant details
- p.Pro66Gln
- rs747459222
- ExAC rs747459222
- TOPMed rs747459222
- gnomAD rs747459222
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.175
- REVEL 0.04
- CADD 16.80
- PolyPhen-2 0.00
- SIFT 0.18
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Middle Eastern population (allele frequency 0.0014)
- Structural context available