Q136K (p.Gln136Lys) variant of TNXB (Tenascin-X)
Q136K (p.Gln136Lys) in TNXB (Tenascin-X) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
Q136K (p.Gln136Lys) variant details
- p.Gln136Lys
- gnomAD rs1445017304
- Missense
- Variant Prioritization Score for Impact Estimate 0.371
- REVEL 0.15
- ESM-1b 1.00
- AlphaMissense 0.22
- CADD 24.30
- PolyPhen-2 0.36
- SIFT 0.03
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available