A36D (p.Ala36Asp) variant of TNXB (Tenascin-X)
A36D (p.Ala36Asp) in TNXB (Tenascin-X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
A36D (p.Ala36Asp) variant details
- p.Ala36Asp
- TOPMed rs1445990247
- gnomAD rs1445990247
- Missense
- Variant Prioritization Score for Impact Estimate 0.229
- REVEL 0.15
- ESM-1b 0.00
- AlphaMissense 0.24
- CADD 22.30
- PolyPhen-2 0.16
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available