F17L (p.Phe17Leu) variant of HNRNPA1 (P09651)
F17L (p.Phe17Leu) in HNRNPA1 (P09651) 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.
F17L (p.Phe17Leu) variant details
- p.Phe17Leu
- rs780033895
- gnomAD 12-54281052-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0957
- CADD 2.13
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available