S4A (p.Ser4Ala) variant of HNRNPA1 (P09651)
S4A (p.Ser4Ala) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data, published literature, and structural context.
S4A (p.Ser4Ala) variant details
- p.Ser4Ala
- gnomAD 12-54281032-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.472
- CADD 8.49
- Most common in the Non-Finnish European population (allele frequency 3.1e-06)
- Structural context available
- Literature evidence available