D169V (p.Asp169Val) variant of INSR (Insulin receptor)
D169V (p.Asp169Val) in INSR (Insulin receptor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
D169V (p.Asp169Val) variant details
- p.Asp169Val
- gnomAD rs1161177676
- Missense
- Variant Prioritization Score for Impact Estimate 0.622
- REVEL 0.70
- MetaLR 0.54
- MetaSVM -0.01
- CADD 23.90
- PolyPhen-2 0.02
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available