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) | ||||||||||
| Deletion | NM_000161.3(GCH1):c.13_19del (p.Pro5fs) | GCH1 | Likely pathogenic | 14 | 55369363 | 55369369 | CGCACAGG | C | criteria provided, single submitter | ClinGen:CA658658257 |
| single nucleotide variant | NM_000161.3(GCH1):c.626+1G>T | GCH1 | Pathogenic | 14 | 55312485 | 55312485 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA389787259 |
| single nucleotide variant | NM_000161.3(GCH1):c.510-1G>C | GCH1 | Pathogenic | 14 | 55313849 | 55313849 | C | G | criteria provided, single submitter | ClinGen:CA389787519 |
| single nucleotide variant | NM_000161.3(GCH1):c.541+1G>C | GCH1 | Pathogenic | 14 | 55313816 | 55313816 | C | G | criteria provided, single submitter | ClinGen:CA389787441 |
| Deletion | NC_000014.9:g.(?_54865307)_(54865456_?)del | GCH1 | Pathogenic | 14 | 55332025 | 55332174 | na | na | criteria provided, single submitter | - |
| single nucleotide variant | NM_000161.3(GCH1):c.344-1G>C | GCH1 | Pathogenic | 14 | 55332155 | 55332155 | C | G | criteria provided, single submitter | ClinGen:CA389790329 |
| 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.1A>T (p.Met1Leu) | GCH1 | Pathogenic | 14 | 55369381 | 55369381 | T | A | criteria provided, single submitter | ClinGen:CA389795046 |
| single nucleotide variant | NM_000161.3(GCH1):c.541+1G>T | GCH1 | Pathogenic | 14 | 55313816 | 55313816 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA389787439 |
| 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 |