Q58H (p.Gln58His) variant of TNXB (Tenascin-X)
Q58H (p.Gln58His) in TNXB (Tenascin-X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
Q58H (p.Gln58His) variant details
- p.Gln58His
- cosmic curated COSV10092
- TOPMed rs1411300342
- gnomAD rs1411300342
- Missense
- Variant Prioritization Score for Impact Estimate 0.284
- REVEL 0.23
- ESM-1b 0.00
- AlphaMissense 0.21
- CADD 22.10
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available