V37I (p.Val37Ile) variant of ABCC8 (Q09428)
V37I (p.Val37Ile) in ABCC8 (Q09428) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
V37I (p.Val37Ile) variant details
- p.Val37Ile
- gnomAD rs1848799538
- Missense
- Variant Prioritization Score for Impact Estimate 0.661
- REVEL 0.59
- CADD 24.60
- PolyPhen-2 0.91
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available