A17V (p.Ala17Val) variant of SLC25A14 (O95258)
A17V (p.Ala17Val) 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 0.38 / 1. The record also includes structural context.
A17V (p.Ala17Val) variant details
- p.Ala17Val
- NCI-TCGA Cosmic COSV9950
- cosmic curated COSV99502
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.381
- REVEL 0.40
- ESM-1b 0.00
- AlphaMissense 0.19
- MetaLR 0.53
- MetaSVM -0.35
- SIFT 0.16
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available