L9M (p.Leu9Met) variant of PDGFRA (P16234)
L9M (p.Leu9Met) in PDGFRA (P16234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
L9M (p.Leu9Met) variant details
- p.Leu9Met
- gnomAD 4-54240056-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.142
- CADD 8.73
- Population evidence available
- Structural context available
- Literature evidence available