S14A (p.Ser14Ala) variant of SLC22A1 (O15245)
S14A (p.Ser14Ala) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
S14A (p.Ser14Ala) variant details
- p.Ser14Ala
- ExAC rs779866607
- gnomAD rs779866607
- Missense
- Variant Prioritization Score for Impact Estimate 0.357
- REVEL 0.29
- CADD 23.00
- PolyPhen-2 0.00
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available