T9I (p.Thr9Ile) variant of TNXB (Tenascin-X)
T9I (p.Thr9Ile) in TNXB (Tenascin-X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
T9I (p.Thr9Ile) variant details
- p.Thr9Ile
- ExAC rs757855203
- gnomAD rs757855203
- Missense
- Variant Prioritization Score for Impact Estimate 0.191
- REVEL 0.05
- ESM-1b 0.00
- AlphaMissense 0.15
- CADD 12.10
- PolyPhen-2 0.00
- SIFT 0.18
- Most common in the South Asian population (allele frequency 1.3e-05)
- Structural context available