P4L (p.Pro4Leu) variant of CDKN1A (P38936)
P4L (p.Pro4Leu) in CDKN1A (P38936) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as benign in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data.
P4L (p.Pro4Leu) variant details
- p.Pro4Leu
- rs4986866
- ClinGen CA3780300
- cosmic curated COSV10879
- ClinVar RCV000952903
- Benign
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.339
- AlphaMissense 0.06
- MetaLR 0.17
- MetaSVM -0.94
- PolyPhen-2 0.00
- SIFT 0.03
- MutPred 0.15
- ClinVar: Benign (not provided)
- EBI: Benign (in dbSNP:rs4986866)
- UniProt: Benign (in dbSNP:rs4986866)
- Population evidence available