Y51H (p.Tyr51His) variant of CDC42 (P60953)
Y51H (p.Tyr51His) in CDC42 (P60953) 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 0.51 / 1. The record also includes structural context.
Y51H (p.Tyr51His) variant details
- p.Tyr51His
- rs1401679863
- NCI-TCGA Cosmic COSV5966
- cosmic curated COSV59663
- gnomAD rs1401679863
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.509
- AlphaMissense 0.83
- MetaLR 0.56
- MetaSVM 0.22
- PolyPhen-2 0.39
- SIFT 0.02
- EVE 0.30
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available