最新の情報は下記 URL でご確認いただけます (外部サイトへ移動します) 。
https://ftp.ncbi.nlm.nih.gov/pub/clinvar/tab_delimited/archive/
表のタイトル行が青色の項目は、クリックすることでソートすることができます。
| Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
|---|---|---|---|---|---|---|---|---|---|---|
| (GRCh37) | ||||||||||
| single nucleotide variant | NM_000161.3(GCH1):c.655C>T (p.Gln219Ter) | GCH1 | Likely pathogenic | 14 | 55310833 | 55310833 | G | A | criteria provided, single submitter | ClinGen:CA389787183 |
| 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.626+1G>A | GCH1 | Pathogenic/Likely pathogenic | 14 | 55312485 | 55312485 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA389787258,OMIM:600225.0019 |
| single nucleotide variant | NM_000161.3(GCH1):c.344-1G>A | GCH1 | Pathogenic | 14 | 55332155 | 55332155 | C | T | criteria provided, single submitter | ClinGen:CA389790328 |
| Indel | NM_000161.3(GCH1):c.186_197delinsA (p.Asp63fs) | GCH1 | Pathogenic | 14 | 55369185 | 55369196 | AGCTCGTTATCC | T | criteria provided, single submitter | ClinGen:CA658798217 |
| single nucleotide variant | NM_000161.3(GCH1):c.614T>A (p.Val205Glu) | GCH1 | Pathogenic/Likely pathogenic | 14 | 55312498 | 55312498 | A | T | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_000161.3(GCH1):c.281C>A (p.Thr94Lys) | GCH1 | Likely pathogenic | 14 | 55369101 | 55369101 | G | T | criteria provided, single submitter | - |
| 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.632T>C (p.Met211Thr) | GCH1 | Likely pathogenic | 14 | 55310856 | 55310856 | A | G | criteria provided, single submitter | - |
| single nucleotide variant | NM_000161.3(GCH1):c.532A>T (p.Arg178Ter) | GCH1 | Pathogenic | 14 | 55313826 | 55313826 | T | A | criteria provided, single submitter | - |