Q97R (p.Gln97Arg) variant of UNC13D (Protein unc-13 homolog D)
Q97R (p.Gln97Arg) in UNC13D (Protein unc-13 homolog D) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
Q97R (p.Gln97Arg) variant details
- p.Gln97Arg
- 1000Genomes rs200891884
- Missense
- Variant Prioritization Score for Impact Estimate 0.0816
- REVEL 0.08
- CADD 1.73
- PolyPhen-2 0.00
- SIFT 0.57
- Most common in the HGDP:YAKUT population (allele frequency 0.04)
- Structural context available