F101C (p.Phe101Cys) variant of SLC22A2 (O15244)
F101C (p.Phe101Cys) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
F101C (p.Phe101Cys) variant details
- p.Phe101Cys
- gnomAD rs1783313764
- Missense
- Variant Prioritization Score for Impact Estimate 0.332
- REVEL 0.19
- CADD 24.30
- PolyPhen-2 0.61
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available