T39M (p.Thr39Met) variant of HNRNPA1 (P09651)
T39M (p.Thr39Met) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
T39M (p.Thr39Met) variant details
- p.Thr39Met
- TOPMed rs1592170668
- Missense
- Variant Prioritization Score for Impact Estimate 0.567
- REVEL 0.42
- CADD 24.10
- PolyPhen-2 0.80
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available