N33D (p.Asn33Asp) variant of PDGFRA (P16234)
N33D (p.Asn33Asp) in PDGFRA (P16234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data, published literature, and structural context.
N33D (p.Asn33Asp) variant details
- p.Asn33Asp
- gnomAD 4-54240074-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.452
- CADD 14.60
- Population evidence available
- Structural context available
- Literature evidence available