N56D (p.Asn56Asp) variant of RAF1 (P04049)
N56D (p.Asn56Asp) in RAF1 (P04049) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
N56D (p.Asn56Asp) variant details
- p.Asn56Asp
- gnomAD 14-20891861-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0771
- REVEL 0.04
- MetaLR 0.06
- MetaSVM -0.97
- CADD 0.01
- PolyPhen-2 0.08
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- RAF1 Raf-like Ras-binding domain domainome 1.0: score -0.559
- Literature evidence available