G38D (p.Gly38Asp) variant of SLC25A14 (O95258)
G38D (p.Gly38Asp) in SLC25A14 (O95258) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
G38D (p.Gly38Asp) variant details
- p.Gly38Asp
- gnomAD X-130345219-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.401
- REVEL 0.32
- ESM-1b 0.00
- AlphaMissense 0.14
- MetaLR 0.31
- MetaSVM -0.63
- CADD 19.70
- Most common in the HGDP:BANTUSOUTHAFRICA population (allele frequency 0.062)
- Structural context available
- Literature evidence available