Description
The Arg256Gly variant in RAF1 has not been reported in the literature nor previo usly identified by our laboratory. However, a different amino acid change at thi s position (Arg256Ser) has been identified in individuals with clinical features of Noonan syndrome, suggesting that a change to this position may not be tolera ted (Pandit 2007). Computational analyses (biochemical amino acid properties, co nservation, AlignGVGD, PolyPhen2, and SIFT) suggest that the Arg256Gly variant m ay impact the protein, though this information is not predictive enough to deter mine pathogenicity. In summary, this variant is likely to be pathogenic, though segregation studies and functional analyses are required to fully establish the pathogenicity of this variant. Individuals with pathogenic variants in exon 7 or 17 in RAF1 have a high incidence of hypertrophic cardiomyopathy (80-95%, Razzaq ue 2007, Pandit 2007). The presence of a heterozygous pathogenic variant in RAF1 is consistent with a diagnosis of Noonan syndrome but this information should b e reconciled with the complete clinical history of this individual.
| # | Sample | Method | Observation |
|---|
| Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
|---|
| 1 | germline | not provided | not provided | not provided | not provided | | 1 | not provided | 1 | not provided |
