R9H (p.Arg9His) variant of CDKN1A (P38936)
R9H (p.Arg9His) in CDKN1A (P38936) 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 0.35 / 1. The record also includes population frequency data.
R9H (p.Arg9His) variant details
- p.Arg9His
- rs143419412
- NCI-TCGA Cosmic COSV5518
- 1000Genomes rs143419412
- ESP rs143419412
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.349
- AlphaMissense 0.09
- MetaLR 0.19
- MetaSVM -0.90
- PolyPhen-2 0.00
- SIFT 0.10
- MutPred 0.21
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available