S39R (p.Ser39Arg) variant of ID3 (Q02535)
S39R (p.Ser39Arg) in ID3 (Q02535) 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, published literature, and structural context.
S39R (p.Ser39Arg) variant details
- p.Ser39Arg
- gnomAD 1-23559310-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.296
- REVEL 0.21
- MetaLR 0.18
- MetaSVM -0.92
- CADD 23.50
- PolyPhen-2 0.04
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available