A36V (p.Ala36Val) variant of CYP4F2 (Cytochrome P450 4F2)
A36V (p.Ala36Val) in CYP4F2 (Cytochrome P450 4F2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
A36V (p.Ala36Val) variant details
- p.Ala36Val
- NCI-TCGA Cosmic COSV9917
- cosmic curated COSV99171
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.246
- REVEL 0.28
- CADD 10.90
- PolyPhen-2 0.01
- SIFT 0.21
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available