G26A (p.Gly26Ala) variant of TNF (Tumor necrosis factor)
G26A (p.Gly26Ala) in TNF (Tumor necrosis factor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
G26A (p.Gly26Ala) variant details
- p.Gly26Ala
- TOPMed rs1271411982
- gnomAD rs1271411982
- Missense
- Variant Prioritization Score for Impact Estimate 0.264
- REVEL 0.23
- CADD 20.20
- PolyPhen-2 0.01
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available