P59S (p.Pro59Ser) variant of HAVCR2 (Q8TDQ0)
P59S (p.Pro59Ser) in HAVCR2 (Q8TDQ0) 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 0.44 / 1. The record also includes population frequency data.
P59S (p.Pro59Ser) variant details
- p.Pro59Ser
- NCI-TCGA Cosmic COSV5715
- cosmic curated COSV57154
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.44
- REVEL 0.32
- CADD 24.90
- PolyPhen-2 0.99
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)