p.Gln39 Arg40insLeuPheLeuAlaProG variant of F2 (Prothrombin)
p.Gln39 Arg40insLeuPheLeuAlaProG in F2 (Prothrombin) 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.
p.Gln39 Arg40insLeuPheLeuAlaProG variant details
- rs755345665
- gnomAD 11-46719314-G-GTG
- Inframe Insertion
- Variant Prioritization Score for Impact Estimate 0.621
- CADD 20.40
- Population evidence available
- Structural context available
- Literature evidence available