P49P (p.Pro49Pro) variant of HNRNPA1 (P09651)
P49P (p.Pro49Pro) in HNRNPA1 (P09651) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
P49P (p.Pro49Pro) variant details
- p.Pro49Pro
- gnomAD 12-54281809-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.163
- CADD 11.60
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available