S30W (p.Ser30Trp) variant of SLC22A2 (O15244)
S30W (p.Ser30Trp) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data and structural context.
S30W (p.Ser30Trp) variant details
- p.Ser30Trp
- ExAC rs774203224
- TOPMed rs774203224
- gnomAD rs774203224
- Missense
- Variant Prioritization Score for Impact Estimate 0.665
- REVEL 0.59
- CADD 25.40
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available