| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Copy number gain | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | HRAS-related condition | |
| | | Single nucleotide variant (synonymous variant +2 more) | HRAS-related condition | |
| | | Single nucleotide variant (synonymous variant +2 more) | HRAS-related condition | |
| | HRAS, LRRC56 (R39W +1 more) | Single nucleotide variant (missense variant) | HRAS-related condition | |
| | | Copy number loss | Autism spectrum disorder | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | HRAS, LRRC56 (T158K +1 more) | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | HRAS, LRRC56 (T158fs +1 more) | Indel (frameshift variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | HRAS, LRRC56 (G115R +1 more) | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | HRAS, LRRC56 (T10A +1 more) | Single nucleotide variant (missense variant) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (P42A +1 more) | Single nucleotide variant (missense variant) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (V125G +1 more) | Single nucleotide variant (missense variant) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (D132G +1 more) | Single nucleotide variant (missense variant) | Costello syndrome | |
| | | Deletion (splice donor variant) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (Q165K +1 more) | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (N93K +1 more) | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (D154Y +1 more) | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (V125fs +1 more) | Deletion (frameshift variant) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | HRAS, LRRC56 (E153* +1 more) | Single nucleotide variant (nonsense +1 more) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (I142del +1 more) | Deletion (inframe_deletion) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (G99S +1 more) | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (S136T +1 more) | Single nucleotide variant (missense variant) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | HRAS, LRRC56 (G101R +1 more) | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (L92V +1 more) | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (intron variant) | Epidermolytic nevus | |
| | | Single nucleotide variant (intron variant) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Deletion | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant (genic upstream transcript variant) | not provided | |
| | | Single nucleotide variant (genic upstream transcript variant) | not provided | |
| | | Duplication (inframe_insertion +1 more) | HRAS-related condition | |
| | | Copy number loss | Beckwith-Wiedemann syndrome due to 11p15 microdeletion | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Deletion | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | C11orf42, MRGPRG +210 more | Copy number gain | Russell-Silver syndrome | |
| | | Single nucleotide variant | not provided | |
| | | Duplication | Neutral lipid storage myopathy | |
| | | Duplication | not provided | |
| | HRAS, LRRC56 (E126* +1 more) | Single nucleotide variant (nonsense +1 more) | Costello syndrome | |
| | HRAS, LRRC56 (I163M +1 more) | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Costello syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Costello syndrome | |