P156L (p.Pro156Leu) variant of SLC6A4 (P31645)
P156L (p.Pro156Leu) in SLC6A4 (P31645) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.87 / 1. The record also includes population frequency data and structural context.
P156L (p.Pro156Leu) variant details
- p.Pro156Leu
- TOPMed rs201940331
- Missense
- Variant Prioritization Score for Impact Estimate 0.874
- REVEL 0.86
- ESM-1b 1.00
- AlphaMissense 0.94
- MetaLR 0.88
- MetaSVM 1.00
- CADD 31.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.7e-05)
- Structural context available