G112D (p.Gly112Asp) variant of TNFRSF4 (P43489)
G112D (p.Gly112Asp) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
G112D (p.Gly112Asp) variant details
- p.Gly112Asp
- TOPMed rs1209627925
- gnomAD rs1209627925
- Missense
- Variant Prioritization Score for Impact Estimate 0.499
- REVEL 0.32
- CADD 23.50
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available