single nucleotide variant | NM_000161.3(GCH1):c.344-1G>A | GCH1 | Pathogenic | 14 | 55332155 | 55332155 | C | T | criteria provided, single submitter | ClinGen:CA389790328 |
Deletion | NC_000014.9:g.(?_54902301)_(54902683_?)del | GCH1 | Pathogenic | 14 | 55369019 | 55369401 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_000161.3(GCH1):c.323G>A (p.Gly108Asp) | GCH1 | Pathogenic | 14 | 55369059 | 55369059 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA120279,UniProtKB:P30793#VAR_016894,OMIM:600225.0012 |
single nucleotide variant | NM_000161.3(GCH1):c.281C>A (p.Thr94Lys) | GCH1 | Likely pathogenic | 14 | 55369101 | 55369101 | G | T | criteria provided, single submitter | - |
Duplication | NM_000161.3(GCH1):c.278dup (p.Thr94fs) | GCH1 | Pathogenic | 14 | 55369103 | 55369104 | C | CT | criteria provided, single submitter | ClinGen:CA658658256 |
single nucleotide variant | NM_000161.3(GCH1):c.274C>A (p.Leu92Ile) | GCH1 | Likely pathogenic | 14 | 55369108 | 55369108 | G | T | criteria provided, single submitter | ClinGen:CA7193645 |
single nucleotide variant | NM_000161.3(GCH1):c.251A>G (p.Glu84Gly) | GCH1 | Likely pathogenic | 14 | 55369131 | 55369131 | T | C | criteria provided, single submitter | - |
Duplication | NM_000161.3(GCH1):c.248dup (p.Glu84fs) | GCH1 | Pathogenic/Likely pathogenic | 14 | 55369133 | 55369134 | G | GC | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000161.3(GCH1):c.220_223del (p.Ala74fs) | GCH1 | Pathogenic | 14 | 55369159 | 55369162 | TAGGC | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000161.3(GCH1):c.212T>C (p.Leu71Pro) | GCH1 | Likely pathogenic | 14 | 55369170 | 55369170 | A | G | criteria provided, single submitter | - |