T39A (p.Thr39Ala) variant of HNRNPA1 (P09651)
T39A (p.Thr39Ala) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data, published literature, and structural context.
T39A (p.Thr39Ala) variant details
- p.Thr39Ala
- gnomAD 12-54281485-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.378
- REVEL 0.28
- CADD 23.20
- PolyPhen-2 0.24
- SIFT 0.09
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available
- Literature evidence available