T9N (p.Thr9Asn) variant of GNAS (P63092)
T9N (p.Thr9Asn) in GNAS (P63092) 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 0.36 / 1. The record also includes population frequency data and structural context.
T9N (p.Thr9Asn) variant details
- p.Thr9Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.362
- REVEL 0.22
- CADD 19.50
- PolyPhen-2 0.02
- SIFT 0.22
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available