A33T (p.Ala33Thr) variant of SLC22A1 (O15245)
A33T (p.Ala33Thr) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
A33T (p.Ala33Thr) variant details
- p.Ala33Thr
- TOPMed rs1348942638
- gnomAD rs1348942638
- Missense
- Variant Prioritization Score for Impact Estimate 0.234
- REVEL 0.12
- CADD 13.70
- PolyPhen-2 0.01
- SIFT 0.39
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available