P32T (p.Pro32Thr) variant of GRM5 (P41594)
P32T (p.Pro32Thr) in GRM5 (P41594) 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 0.54 / 1. The record also includes population frequency data.
P32T (p.Pro32Thr) variant details
- p.Pro32Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.542
- REVEL 0.44
- MetaLR 0.57
- MetaSVM 0.12
- CADD 20.40
- PolyPhen-2 0.15
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available