| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 8 +1 more | |
| | | Single nucleotide variant (missense variant) | RASopathy +6 more | |
| | | Single nucleotide variant (missense variant) | RASopathy +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Noonan syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 8 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 8 | |
Click to view in NCBI Gene