A71V (p.Ala71Val) variant of HNRNPA1 (P09651)
A71V (p.Ala71Val) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
A71V (p.Ala71Val) variant details
- p.Ala71Val
- gnomAD rs1357903521
- Missense
- Variant Prioritization Score for Impact Estimate 0.497
- REVEL 0.29
- CADD 25.70
- PolyPhen-2 0.80
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available