W37S (p.Trp37Ser) variant of HNRNPA1 (P09651)
W37S (p.Trp37Ser) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data, published literature, and structural context.
W37S (p.Trp37Ser) variant details
- p.Trp37Ser
- gnomAD 12-54281480-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.635
- REVEL 0.49
- CADD 33.00
- PolyPhen-2 0.99
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available