V26A (p.Val26Ala) variant of SLC6A4 (P31645)
V26A (p.Val26Ala) in SLC6A4 (P31645) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
V26A (p.Val26Ala) variant details
- p.Val26Ala
- ESP rs375503605
- ExAC rs375503605
- TOPMed rs375503605
- gnomAD rs375503605
- Missense
- Variant Prioritization Score for Impact Estimate 0.237
- REVEL 0.12
- ESM-1b 0.00
- AlphaMissense 0.10
- MetaLR 0.13
- MetaSVM -0.99
- CADD 13.40
- Most common in the HGDP:SAN population (allele frequency 0.25)
- Structural context available