D36G (p.Asp36Gly) variant of TNFRSF1A (P19438)
D36G (p.Asp36Gly) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
D36G (p.Asp36Gly) variant details
- p.Asp36Gly
- gnomAD rs1948089106
- Missense
- Variant Prioritization Score for Impact Estimate 0.552
- REVEL 0.63
- CADD 22.20
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available