H21N (p.His21Asn) variant of TNFRSF1B (P20333)
H21N (p.His21Asn) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
H21N (p.His21Asn) variant details
- p.His21Asn
- gnomAD 1-12167152-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.276
- REVEL 0.18
- MetaLR 0.63
- MetaSVM -0.33
- CADD 10.90
- PolyPhen-2 0.01
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 2.1e-06)
- Structural context available
- Literature evidence available