S32T (p.Ser32Thr) variant of HNRNPA1 (P09651)
S32T (p.Ser32Thr) 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 and structural context.
S32T (p.Ser32Thr) variant details
- p.Ser32Thr
- TOPMed rs1466891120
- gnomAD rs1466891120
- Missense
- Variant Prioritization Score for Impact Estimate 0.471
- REVEL 0.28
- CADD 23.60
- PolyPhen-2 0.19
- SIFT 0.01
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available