P41R (p.Pro41Arg) variant of TNXB (Tenascin-X)
P41R (p.Pro41Arg) in TNXB (Tenascin-X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
P41R (p.Pro41Arg) variant details
- p.Pro41Arg
- ExAC rs769084817
- TOPMed rs769084817
- gnomAD rs769084817
- Missense
- Variant Prioritization Score for Impact Estimate 0.438
- REVEL 0.31
- ESM-1b 0.00
- AlphaMissense 0.12
- CADD 25.10
- PolyPhen-2 0.60
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available