A79T (p.Ala79Thr) variant of PTPN2 (P17706)
A79T (p.Ala79Thr) in PTPN2 (P17706) 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 0.58 / 1. The record also includes population frequency data and structural context.
A79T (p.Ala79Thr) variant details
- p.Ala79Thr
- NCI-TCGA Cosmic COSV5899
- cosmic curated COSV58995
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.584
- REVEL 0.44
- CADD 25.30
- PolyPhen-2 0.95
- SIFT 0.04
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available