Q13H (p.Gln13His) variant of SLC18A2 (Q05940)
Q13H (p.Gln13His) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data, published literature, and structural context.
Q13H (p.Gln13His) variant details
- p.Gln13His
- gnomAD 10-117241732-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.532
- CADD 17.10
- PolyPhen-2 0.00
- SIFT 0.13
- Population evidence available
- Structural context available
- Literature evidence available