P37T (p.Pro37Thr) variant of ID3 (Q02535)
P37T (p.Pro37Thr) in ID3 (Q02535) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data, published literature, and structural context.
P37T (p.Pro37Thr) variant details
- p.Pro37Thr
- gnomAD 1-23559318-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.495
- REVEL 0.45
- MetaLR 0.27
- MetaSVM -0.65
- CADD 23.10
- PolyPhen-2 0.14
- SIFT 0.09
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available