S39F (p.Ser39Phe) variant of SLC22A5 (O76082)
S39F (p.Ser39Phe) in SLC22A5 (O76082) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
S39F (p.Ser39Phe) variant details
- p.Ser39Phe
- gnomAD rs1350319349
- Missense
- Variant Prioritization Score for Impact Estimate 0.211
- REVEL 0.24
- CADD 15.60
- PolyPhen-2 0.00
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available