W97C (p.Trp97Cys) variant of SLC2A2 (P11168)
W97C (p.Trp97Cys) in SLC2A2 (P11168) 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 0.85 / 1. The record also includes structural context.
W97C (p.Trp97Cys) variant details
- p.Trp97Cys
- rs1407375423
- TOPMed rs1407375423
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.848
- AlphaMissense 0.94
- MetaLR 0.76
- MetaSVM 0.77
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.97
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available