L16I (p.Leu16Ile) variant of INS (Insulin)
L16I (p.Leu16Ile) in INS (Insulin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
L16I (p.Leu16Ile) variant details
- p.Leu16Ile
- gnomAD 11-2160926-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.322
- REVEL 0.31
- MetaLR 0.49
- MetaSVM -0.39
- CADD 12.20
- PolyPhen-2 0.05
- SIFT 0.19
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available