p.Thr13 Phe19del variant of HNRNPA1 (P09651)
p.Thr13 Phe19del in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
p.Thr13 Phe19del variant details
- gnomAD 12-54281057-GCACA
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.131
- CADD 7.08
- Most common in the Latino/Admixed American population (allele frequency 2.9e-05)
- Structural context available
- Literature evidence available