P37Q (p.Pro37Gln) variant of ID3 (Q02535)
P37Q (p.Pro37Gln) in ID3 (Q02535) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data, published literature, and structural context.
P37Q (p.Pro37Gln) variant details
- p.Pro37Gln
- gnomAD 1-23559317-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.557
- REVEL 0.46
- MetaLR 0.41
- MetaSVM -0.43
- CADD 25.00
- PolyPhen-2 0.98
- SIFT 0.22
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available