V27I (p.Val27Ile) variant of TNFRSF1A (P19438)
V27I (p.Val27Ile) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
V27I (p.Val27Ile) variant details
- p.Val27Ile
- TOPMed rs1182623871
- gnomAD rs1182623871
- Missense
- Variant Prioritization Score for Impact Estimate 0.528
- REVEL 0.49
- CADD 22.50
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available