A36V (p.Ala36Val) variant of TNXB (Tenascin-X)
A36V (p.Ala36Val) in TNXB (Tenascin-X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
A36V (p.Ala36Val) variant details
- p.Ala36Val
- cosmic curated COSV10749
- TOPMed rs1445990247
- gnomAD rs1445990247
- Missense
- Variant Prioritization Score for Impact Estimate 0.181
- REVEL 0.06
- ESM-1b 0.00
- AlphaMissense 0.11
- CADD 21.90
- PolyPhen-2 0.00
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available