| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiofaciocutaneous syndrome 1 | |
| | | Microsatellite (intron variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +8 more | |
| | | Single nucleotide variant (synonymous variant) | RASopathy +8 more | |
| | | Single nucleotide variant (intron variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +7 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | RASopathy +7 more | |
| | | Single nucleotide variant (intron variant) | RASopathy +7 more | |
| | | Deletion (intron variant) | RASopathy +7 more | |
| | | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +7 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Lung cancer +7 more | |
| | | Insertion (intron variant) | Cardiofaciocutaneous syndrome 1 +8 more | |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 | |
| | BRAF, LOC126860202 (R266Q +4 more) | Single nucleotide variant (missense variant) | LEOPARD syndrome 3 +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +8 more | |
| | | Single nucleotide variant (intron variant) | Lung cancer +8 more | |
| | | Single nucleotide variant (synonymous variant) | RASopathy +8 more | |
| | | Single nucleotide variant (synonymous variant) | Noonan syndrome 1 +7 more | |
| | | Single nucleotide variant (synonymous variant) | LEOPARD syndrome 3 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LEOPARD syndrome 3 +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | Cardiofaciocutaneous syndrome 1 | |
| | | Deletion (frameshift variant) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (intron variant) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | RASopathy +7 more | |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (missense variant) | RASopathy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RASopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RASopathy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (synonymous variant) | RASopathy +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | LEOPARD syndrome 3 +10 more | |
| | | Single nucleotide variant (missense variant) | RASopathy +2 more | |
| | | Single nucleotide variant (intron variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | LEOPARD syndrome 3 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | LEOPARD syndrome 3 +8 more | |
| | | Single nucleotide variant (intron variant) | Cardiofaciocutaneous syndrome 1 +8 more | |
| | | Single nucleotide variant (intron variant) | RASopathy +9 more | |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome and Noonan-related syndrome +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +7 more | GConflicting classifications of pathogenicity |
| | BRAF, LOC126860202 (I342V +4 more) | Single nucleotide variant (missense variant) | RASopathy | |
| | | 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) | Noonan syndrome and Noonan-related syndrome | |
| | | Single nucleotide variant (intron variant) | Noonan syndrome 1 +8 more | |
| | | Single nucleotide variant (intron variant) | Noonan syndrome 1 +8 more | |
| | | Single nucleotide variant (intron variant) | not specified +8 more | |
| | | Single nucleotide variant (missense variant) | KRAS-related disorder +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma, cutaneous malignant, susceptibility to, 1 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Lung cancer +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +10 more | |
| | | 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 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Noonan syndrome 7 +8 more | |
| | | Single nucleotide variant (intron variant) | RASopathy | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Noonan syndrome 7 +8 more | |
| | | 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) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiofaciocutaneous syndrome 1 | |
| | | Single nucleotide variant (missense variant) | RASopathy | |
| | | 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) | RASopathy +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Noonan syndrome 7 +9 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome and Noonan-related syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +10 more | |
| | | Single nucleotide variant (missense variant) | Noonan syndrome 7 +7 more | |
| | | Single nucleotide variant (missense variant) | RASopathy +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardio-facio-cutaneous syndrome +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +7 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) | Noonan syndrome and Noonan-related syndrome +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 | |