T38M (p.Thr38Met) variant of CYP4F2 (Cytochrome P450 4F2)
T38M (p.Thr38Met) in CYP4F2 (Cytochrome P450 4F2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data, published literature, and structural context.
T38M (p.Thr38Met) variant details
- p.Thr38Met
- rs533748322
- gnomAD 19-15879423-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0618
- CADD 0.27
- SIFT 0.48
- Most common in the 1KG:LWK population (allele frequency 0.0058)
- Structural context available
- Literature evidence available