G26D (p.Gly26Asp) variant of TNF (Tumor necrosis factor)
G26D (p.Gly26Asp) in TNF (Tumor necrosis factor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
G26D (p.Gly26Asp) variant details
- p.Gly26Asp
- TOPMed rs1271411982
- gnomAD rs1271411982
- Missense
- Variant Prioritization Score for Impact Estimate 0.254
- REVEL 0.23
- CADD 16.90
- PolyPhen-2 0.03
- SIFT 0.17
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available