G116R (p.Gly116Arg) variant of TNXB (Tenascin-X)
G116R (p.Gly116Arg) in TNXB (Tenascin-X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
G116R (p.Gly116Arg) variant details
- p.Gly116Arg
- Ensembl rs1780499152
- Missense
- Variant Prioritization Score for Impact Estimate 0.546
- REVEL 0.41
- ESM-1b 1.00
- AlphaMissense 0.55
- CADD 24.30
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available