V167M (p.Val167Met) variant of INSR (Insulin receptor)
V167M (p.Val167Met) in INSR (Insulin receptor) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data and structural context.
V167M (p.Val167Met) variant details
- p.Val167Met
- cosmic curated COSV57161
- TOPMed rs938519025
- Missense
- Variant Prioritization Score for Impact Estimate 0.642
- REVEL 0.55
- MetaLR 0.69
- MetaSVM 0.43
- CADD 23.60
- PolyPhen-2 0.92
- SIFT 0.02
- Most common in the African/African-American population (allele frequency 6e-05)
- Structural context available