G38V (p.Gly38Val) variant of SLC25A14 (O95258)
G38V (p.Gly38Val) in SLC25A14 (O95258) 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 0.42 / 1. The record also includes population frequency data and structural context.
G38V (p.Gly38Val) variant details
- p.Gly38Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.415
- REVEL 0.34
- ESM-1b 0.00
- AlphaMissense 0.10
- MetaLR 0.33
- MetaSVM -0.62
- CADD 20.60
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available