G25V (p.Gly25Val) variant of SLC6A4 (P31645)
G25V (p.Gly25Val) in SLC6A4 (P31645) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
G25V (p.Gly25Val) variant details
- p.Gly25Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.366
- REVEL 0.26
- ESM-1b 0.00
- AlphaMissense 0.18
- MetaLR 0.18
- MetaSVM -0.80
- CADD 22.30
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Latino/Admixed American population (allele frequency 6.6e-05)
- Structural context available