H33Y (p.His33Tyr) variant of TNFRSF1A (P19438)
H33Y (p.His33Tyr) in TNFRSF1A (P19438) 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 0.57 / 1. The record also includes population frequency data and structural context.
H33Y (p.His33Tyr) variant details
- p.His33Tyr
- rs1005685583
- NCI-TCGA Cosmic COSV9936
- cosmic curated COSV99369
- Ensembl rs1005685583
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.573
- REVEL 0.48
- CADD 13.20
- PolyPhen-2 0.25
- SIFT 0.48
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available