D27del (p.Asp27del) variant of HNRNPA1 (P09651)
D27del (p.Asp27del) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.74 / 1. The record also includes population frequency data, published literature, and structural context.
D27del (p.Asp27del) variant details
- gnomAD 12-54281447-CTGA-
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.742
- CADD 22.60
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available