T116I (p.Thr116Ile) variant of UNC13D (Protein unc-13 homolog D)
T116I (p.Thr116Ile) in UNC13D (Protein unc-13 homolog D) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data and structural context.
T116I (p.Thr116Ile) variant details
- p.Thr116Ile
- TOPMed rs2064959011
- gnomAD rs2064959011
- Missense
- Variant Prioritization Score for Impact Estimate 0.69
- REVEL 0.60
- CADD 32.00
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available