V38M (p.Val38Met) variant of SLC6A4 (P31645)
V38M (p.Val38Met) 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.
V38M (p.Val38Met) variant details
- p.Val38Met
- gnomAD rs1169264519
- Missense
- Variant Prioritization Score for Impact Estimate 0.115
- REVEL 0.03
- ESM-1b 0.00
- AlphaMissense 0.08
- MetaLR 0.09
- MetaSVM -0.97
- CADD 3.15
- Most common in the HGDP:SAN population (allele frequency 1)
- Structural context available