N88D (p.Asn88Asp) variant of TNFRSF4 (P43489)
N88D (p.Asn88Asp) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data.
N88D (p.Asn88Asp) variant details
- p.Asn88Asp
- TOPMed rs1649313437
- gnomAD rs1649313437
- Missense
- Variant Prioritization Score for Impact Estimate 0.362
- REVEL 0.26
- CADD 21.90
- PolyPhen-2 0.65
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)