F49del (p.Phe49del) variant of INS (Insulin)
F49del (p.Phe49del) in INS (Insulin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
F49del (p.Phe49del) variant details
- rs1376385292
- gnomAD 11-2160823-TAGA-T
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.409
- CADD 17.20
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available