| | | Deletion | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Indel (splice donor variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Deletion (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Deletion (frameshift variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant +1 more) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Deletion (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (nonsense) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Duplication | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant +1 more) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant +1 more) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant +1 more) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (intron variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (synonymous variant) | Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |