| | | Single nucleotide variant (missense variant) | Neoplasm | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 8 +2 more | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | RASopathy +1 more | |
| | | Deletion (inframe_deletion) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Deletion (inframe_deletion) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 4 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Melanoma +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Duplication (intron variant) | Cardio-facio-cutaneous syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Indel (intron variant) | Cardio-facio-cutaneous syndrome +2 more | |
| | | Deletion (intron variant) | Cardio-facio-cutaneous syndrome +2 more | |
| | | Deletion (intron variant) | Cardio-facio-cutaneous syndrome +2 more | |
| | | Deletion (3 prime UTR variant +1 more) | Noonan syndrome +1 more | |
| | | Duplication (3 prime UTR variant +1 more) | Noonan syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (3 prime UTR variant +1 more) | Noonan syndrome +1 more | |
| | | Microsatellite (5 prime UTR variant) | Cardio-facio-cutaneous syndrome +2 more | |
| | | Microsatellite (5 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome +1 more | |
| | | Duplication (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome +1 more | |
| | | Insertion (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Duplication (3 prime UTR variant) | Noonan syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Noonan syndrome +1 more | |
| | | Deletion (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Duplication (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Duplication (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Deletion (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Deletion (3 prime UTR variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Deletion (3 prime UTR variant) | Noonan syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (inframe_deletion) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 1 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Noonan syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Noonan syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | RASopathy +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +8 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (intron variant) | RASopathy | |
| | | Single nucleotide variant (nonsense +1 more) | Cardio-facio-cutaneous syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Noonan syndrome and Noonan-related syndrome | |
| | | Deletion (intron variant) | Cardio-facio-cutaneous syndrome +5 more | |
| | | Duplication (intron variant) | Cardio-facio-cutaneous syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental delay +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (3 prime UTR variant +2 more) | RASopathy | |
| | | Single nucleotide variant (missense variant) | RASopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | RASopathy +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | RASopathy +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Noonan syndrome and Noonan-related syndrome | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome and Noonan-related syndrome | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | RASopathy +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +13 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +5 more | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome | |