P56L (p.Pro56Leu) variant of NTRK2 (Q16620)
P56L (p.Pro56Leu) in NTRK2 (Q16620) 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 0.79 / 1. The record also includes population frequency data and structural context.
P56L (p.Pro56Leu) variant details
- p.Pro56Leu
- NCI-TCGA Cosmic COSV5287
- cosmic curated COSV52871
- Ensembl rs2058659300
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.794
- REVEL 0.81
- CADD 25.10
- PolyPhen-2 1.00
- SIFT 0.10
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available