A26T (p.Ala26Thr) variant of PLK1 (P53350)
A26T (p.Ala26Thr) in PLK1 (P53350) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
A26T (p.Ala26Thr) variant details
- p.Ala26Thr
- ExAC rs758028407
- TOPMed rs758028407
- gnomAD rs758028407
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.26
- REVEL 0.15
- CADD 21.70
- PolyPhen-2 0.00
- SIFT 0.01
- ClinVar: Uncertain significance (not specified)
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 0.00013)
- Structural context available