T122A (p.Thr122Ala) variant of TNXB (Tenascin-X)
T122A (p.Thr122Ala) in TNXB (Tenascin-X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
T122A (p.Thr122Ala) variant details
- p.Thr122Ala
- TOPMed rs1411732850
- gnomAD rs1411732850
- Missense
- Variant Prioritization Score for Impact Estimate 0.166
- REVEL 0.18
- ESM-1b 0.00
- AlphaMissense 0.07
- CADD 10.80
- PolyPhen-2 0.37
- SIFT 0.06
- Most common in the South Asian population (allele frequency 2.8e-05)
- Structural context available