| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_indel +1 more) | Noonan syndrome 9 | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 9 | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 9 | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 9 | |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 9 | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 9 | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Noonan syndrome 9 | |
Click to view in NCBI Gene