P7L (p.Pro7Leu) variant of HNRNPA1 (P09651)
P7L (p.Pro7Leu) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and structural context.
P7L (p.Pro7Leu) variant details
- p.Pro7Leu
- ExAC rs766224014
- gnomAD rs766224014
- Missense
- Variant Prioritization Score for Impact Estimate 0.584
- REVEL 0.46
- CADD 24.80
- PolyPhen-2 0.41
- SIFT 0.04
- Most common in the Latino/Admixed American population (allele frequency 2.4e-05)
- Structural context available