S29G (p.Ser29Gly) variant of HNRNPA1 (P09651)
S29G (p.Ser29Gly) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data, published literature, and structural context.
S29G (p.Ser29Gly) variant details
- p.Ser29Gly
- gnomAD 12-54281455-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.62
- REVEL 0.59
- CADD 29.20
- PolyPhen-2 0.77
- SIFT 0.03
- Population evidence available
- Structural context available
- Literature evidence available