G26A (p.Gly26Ala) variant of TNFRSF1A (P19438)
G26A (p.Gly26Ala) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
G26A (p.Gly26Ala) variant details
- p.Gly26Ala
- gnomAD rs1259443563
- Missense
- Variant Prioritization Score for Impact Estimate 0.422
- REVEL 0.55
- CADD 14.90
- PolyPhen-2 0.19
- SIFT 0.08
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available