F17F (p.Phe17Phe) variant of HNRNPA1 (P09651)
F17F (p.Phe17Phe) in HNRNPA1 (P09651) is a synonymous 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.
F17F (p.Phe17Phe) variant details
- p.Phe17Phe
- rs780033895
- gnomAD 12-54281052-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0999
- CADD 2.72
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available
- Literature evidence available