G39S (p.Gly39Ser) variant of SLC22A2 (O15244)
G39S (p.Gly39Ser) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
G39S (p.Gly39Ser) variant details
- p.Gly39Ser
- ExAC rs756963059
- TOPMed rs756963059
- gnomAD rs756963059
- Missense
- Variant Prioritization Score for Impact Estimate 0.633
- REVEL 0.53
- CADD 24.20
- PolyPhen-2 1.00
- SIFT 0.10
- Most common in the REMAINING population (allele frequency 5e-05)
- Structural context available