V37I (p.Val37Ile) variant of NOS1AP (O75052)
V37I (p.Val37Ile) in NOS1AP (O75052) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
V37I (p.Val37Ile) variant details
- p.Val37Ile
- cosmic curated COSV62632
- ESP rs141560292
- ExAC rs141560292
- TOPMed rs141560292
- Missense
- Variant Prioritization Score for Impact Estimate 0.347
- REVEL 0.11
- CADD 17.50
- PolyPhen-2 0.01
- SIFT 1.00
- Most common in the REMAINING population (allele frequency 0.00047)
- Structural context available