T87A (p.Thr87Ala) variant of KRT17 (Keratin, type I cytoskeletal 17)
T87A (p.Thr87Ala) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
T87A (p.Thr87Ala) variant details
- p.Thr87Ala
- gnomAD 17-41620491-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.1
- CADD 2.75
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available
- Literature evidence available