V37I (p.Val37Ile) variant of PON1 (Serum paraoxonase/arylesterase 1)
V37I (p.Val37Ile) in PON1 (Serum paraoxonase/arylesterase 1) is a missense change. Clinical records from ClinVar and UniProt describe it as likely benign in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
V37I (p.Val37Ile) variant details
- p.Val37Ile
- rs987766326
- NCI-TCGA Cosmic COSV5593
- 1000Genomes rs987766326
- TOPMed rs987766326
- Likely benign
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.122
- REVEL 0.05
- CADD 1.15
- PolyPhen-2 0.00
- SIFT 0.20
- ClinVar: Likely benign (not specified)
- UniProt: Likely benign
- Most common in the Latino/Admixed American population (allele frequency 6.7e-05)
- Structural context available