Q111H (p.Gln111His) variant of SLC6A4 (P31645)
Q111H (p.Gln111His) in SLC6A4 (P31645) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
Q111H (p.Gln111His) variant details
- p.Gln111His
- ExAC rs778131401
- gnomAD rs778131401
- Missense
- Variant Prioritization Score for Impact Estimate 0.565
- REVEL 0.54
- ESM-1b 0.99
- AlphaMissense 0.54
- MetaLR 0.55
- MetaSVM 0.14
- CADD 24.50
- Most common in the Latino/Admixed American population (allele frequency 0.00011)
- Structural context available