A22G (p.Ala22Gly) variant of INS (Insulin)
A22G (p.Ala22Gly) in INS (Insulin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data, published literature, and structural context.
A22G (p.Ala22Gly) variant details
- p.Ala22Gly
- gnomAD 11-2160907-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.352
- REVEL 0.35
- MetaLR 0.88
- MetaSVM 0.57
- CADD 6.99
- PolyPhen-2 0.00
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available