P37R (p.Pro37Arg) variant of ID3 (Q02535)
P37R (p.Pro37Arg) in ID3 (Q02535) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data, published literature, and structural context.
P37R (p.Pro37Arg) variant details
- p.Pro37Arg
- gnomAD 1-23559317-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.618
- REVEL 0.54
- MetaLR 0.52
- MetaSVM 0.04
- CADD 28.70
- PolyPhen-2 0.97
- SIFT 0.01
- Most common in the Latino/Admixed American population (allele frequency 6.7e-05)
- Structural context available
- Literature evidence available