S14P (p.Ser14Pro) variant of SLC22A1 (O15245)
S14P (p.Ser14Pro) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
S14P (p.Ser14Pro) variant details
- p.Ser14Pro
- ExAC rs779866607
- gnomAD rs779866607
- Missense
- Variant Prioritization Score for Impact Estimate 0.373
- REVEL 0.31
- CADD 23.40
- PolyPhen-2 0.00
- SIFT 0.00
- Most common in the South Asian population (allele frequency 3.5e-05)
- Structural context available