Y69F (p.Tyr69Phe) variant of TNFRSF1A (P19438)
Y69F (p.Tyr69Phe) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
Y69F (p.Tyr69Phe) variant details
- p.Tyr69Phe
- gnomAD rs1948084832
- Missense
- Variant Prioritization Score for Impact Estimate 0.277
- REVEL 0.31
- CADD 12.80
- PolyPhen-2 0.14
- SIFT 0.33
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available