P2S (p.Pro2Ser) variant of SLC22A2 (O15244)
P2S (p.Pro2Ser) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
P2S (p.Pro2Ser) variant details
- p.Pro2Ser
- TOPMed rs1346240034
- gnomAD rs1346240034
- Missense
- Variant Prioritization Score for Impact Estimate 0.226
- REVEL 0.15
- CADD 17.90
- PolyPhen-2 0.20
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available