V31F (p.Val31Phe) variant of SLC6A4 (P31645)
V31F (p.Val31Phe) in SLC6A4 (P31645) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
V31F (p.Val31Phe) variant details
- p.Val31Phe
- ExAC rs747721432
- TOPMed rs747721432
- gnomAD rs747721432
- Missense
- Variant Prioritization Score for Impact Estimate 0.154
- REVEL 0.05
- ESM-1b 0.00
- AlphaMissense 0.07
- MetaLR 0.11
- MetaSVM -0.97
- CADD 8.50
- Most common in the African/African-American population (allele frequency 9.7e-05)
- Structural context available