L13P (p.Leu13Pro) variant of INS (Insulin)
L13P (p.Leu13Pro) in INS (Insulin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes population frequency data and structural context.
L13P (p.Leu13Pro) variant details
- p.Leu13Pro
- gnomAD rs1313490068
- Missense
- Variant Prioritization Score for Impact Estimate 0.704
- REVEL 0.76
- MetaLR 0.77
- MetaSVM 0.52
- CADD 25.30
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available