T69A (p.Thr69Ala) variant of SLC6A4 (P31645)
T69A (p.Thr69Ala) in SLC6A4 (P31645) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
T69A (p.Thr69Ala) variant details
- p.Thr69Ala
- gnomAD rs1230700471
- Missense
- Variant Prioritization Score for Impact Estimate 0.117
- REVEL 0.08
- ESM-1b 0.00
- AlphaMissense 0.06
- MetaLR 0.16
- MetaSVM -0.97
- CADD 1.84
- Most common in the 1KG:MSL population (allele frequency 0.31)
- Structural context available