P13T (p.Pro13Thr) variant of GRIN2A (Q12879)
P13T (p.Pro13Thr) in GRIN2A (Q12879) is a missense change. 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.
P13T (p.Pro13Thr) variant details
- p.Pro13Thr
- gnomAD rs1201806901
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- REVEL 0.10
- CADD 18.80
- PolyPhen-2 0.01
- SIFT 0.41
- Population evidence available
- Structural context available