P34R (p.Pro34Arg) variant of HRAS (GTPase HRas)
P34R (p.Pro34Arg) in HRAS (GTPase HRas) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes population frequency data and structural context.
P34R (p.Pro34Arg) variant details
- p.Pro34Arg
- Ensembl rs2133994210
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.702
- REVEL 0.85
- AlphaMissense 0.99
- MetaLR 0.68
- MetaSVM 0.63
- CADD 26.80
- PolyPhen-2 1.00
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available