L13M (p.Leu13Met) variant of HNRNPA1 (P09651)
L13M (p.Leu13Met) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data, published literature, and structural context.
L13M (p.Leu13Met) variant details
- p.Leu13Met
- gnomAD 12-54281407-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.533
- REVEL 0.47
- CADD 26.30
- PolyPhen-2 0.98
- SIFT 0.01
- Population evidence available
- Structural context available
- Literature evidence available