P112H (p.Pro112His) variant of ANKRD1 (Q15327)
P112H (p.Pro112His) in ANKRD1 (Q15327) 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 0.37 / 1. The record also includes population frequency data and structural context.
P112H (p.Pro112His) variant details
- p.Pro112His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.374
- REVEL 0.29
- CADD 24.70
- PolyPhen-2 0.25
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available