P37S (p.Pro37Ser) variant of ID3 (Q02535)
P37S (p.Pro37Ser) 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.
P37S (p.Pro37Ser) variant details
- p.Pro37Ser
- gnomAD 1-23559318-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.556
- REVEL 0.53
- MetaLR 0.44
- MetaSVM -0.15
- CADD 25.00
- PolyPhen-2 0.71
- SIFT 0.11
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available
- Literature evidence available