P15S (p.Pro15Ser) variant of SLCO1B1 (Q9Y6L6)
P15S (p.Pro15Ser) in SLCO1B1 (Q9Y6L6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data and structural context.
P15S (p.Pro15Ser) variant details
- p.Pro15Ser
- TOPMed rs1940309779
- gnomAD rs1940309779
- Missense
- Variant Prioritization Score for Impact Estimate 0.0505
- REVEL 0.03
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 0.82
- Most common in the Non-Finnish European population (allele frequency 3.4e-06)
- Structural context available