P16S (p.Pro16Ser) variant of SLC22A5 (O76082)
P16S (p.Pro16Ser) in SLC22A5 (O76082) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
P16S (p.Pro16Ser) variant details
- p.Pro16Ser
- gnomAD 5-132370018-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.509
- REVEL 0.49
- CADD 22.60
- PolyPhen-2 0.27
- SIFT 0.08
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available
- Literature evidence available