P49A (p.Pro49Ala) variant of HNRNPA1 (P09651)
P49A (p.Pro49Ala) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data and structural context.
P49A (p.Pro49Ala) variant details
- p.Pro49Ala
- 1000Genomes rs566750529
- Missense
- Variant Prioritization Score for Impact Estimate 0.685
- REVEL 0.62
- CADD 25.80
- PolyPhen-2 0.72
- SIFT 0.01
- Most common in the 1KG:STU population (allele frequency 0.0051)
- Structural context available