T39T (p.Thr39Thr) variant of HNRNPA1 (P09651)
T39T (p.Thr39Thr) in HNRNPA1 (P09651) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
T39T (p.Thr39Thr) variant details
- p.Thr39Thr
- gnomAD 12-54281487-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.144
- CADD 8.98
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available