N25S (p.Asn25Ser) variant of SLCO1B1 (Q9Y6L6)
N25S (p.Asn25Ser) in SLCO1B1 (Q9Y6L6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
N25S (p.Asn25Ser) variant details
- p.Asn25Ser
- TOPMed rs1236489495
- Missense
- Variant Prioritization Score for Impact Estimate 0.131
- REVEL 0.06
- CADD 13.80
- PolyPhen-2 0.00
- SIFT 0.25
- Most common in the Middle Eastern population (allele frequency 0.0011)
- Structural context available