P16H (p.Pro16His) variant of SLC22A5 (O76082)
P16H (p.Pro16His) in SLC22A5 (O76082) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
P16H (p.Pro16His) variant details
- p.Pro16His
- gnomAD 5-132370019-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.398
- REVEL 0.46
- CADD 21.30
- PolyPhen-2 0.05
- SIFT 0.09
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available