L16V (p.Leu16Val) variant of HNRNPA1 (P09651)
L16V (p.Leu16Val) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
L16V (p.Leu16Val) variant details
- p.Leu16Val
- ExAC rs754983468
- gnomAD rs754983468
- Missense
- Variant Prioritization Score for Impact Estimate 0.0803
- CADD 0.03
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available