p.Ile56 Tyr57del variant of CSRP3 (P50461)
p.Ile56 Tyr57del in CSRP3 (P50461) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data, published literature, and structural context.
p.Ile56 Tyr57del variant details
- gnomAD 11-19188245-AGTAG
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.545
- CADD 16.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available