G6W (p.Gly6Trp) variant of ACADM (P11310)
G6W (p.Gly6Trp) in ACADM (P11310) 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 0.30 / 1. The record also includes population frequency data and structural context.
G6W (p.Gly6Trp) variant details
- p.Gly6Trp
- NCI-TCGA Cosmic COSV1008
- cosmic curated COSV10089
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.295
- REVEL 0.29
- CADD 14.70
- PolyPhen-2 0.01
- SIFT 0.08
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available