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_000531.6(OTC):c.673C>T (p.Pro225Ser) | OTC | Likely pathogenic | X | 38268004 | 38268004 | C | T | criteria provided, single submitter | ClinGen:CA327910816 |
| single nucleotide variant | NM_000531.6(OTC):c.298+2T>G | OTC | Pathogenic | X | 38229132 | 38229132 | T | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA412717048 |
| single nucleotide variant | NM_000531.6(OTC):c.494A>G (p.Asp165Gly) | OTC | Likely pathogenic | X | 38260635 | 38260635 | A | G | criteria provided, single submitter | ClinGen:CA412723703 |
| single nucleotide variant | NM_000531.6(OTC):c.540+1G>T | OTC | Pathogenic | X | 38260682 | 38260682 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA412724240 |
| single nucleotide variant | NM_000531.6(OTC):c.540+265G>A | OTC | Pathogenic | X | 38260946 | 38260946 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA658658977 |
| single nucleotide variant | NM_000531.5(OTC):c.-142G>A | OTC | Likely pathogenic | X | 38211808 | 38211808 | G | A | criteria provided, single submitter | ClinGen:CA658799698 |
| single nucleotide variant | NM_000531.6(OTC):c.228A>C (p.Leu76Phe) | OTC | Likely pathogenic | X | 38229060 | 38229060 | A | C | criteria provided, single submitter | ClinGen:CA412716809 |
| single nucleotide variant | NM_000531.6(OTC):c.593A>G (p.Asn198Ser) | OTC | Pathogenic | X | 38262923 | 38262923 | A | G | criteria provided, single submitter | ClinGen:CA412725470 |
| Deletion | NC_000023.11:g.(?_38381322)_(38413090_?)del | OTC | Pathogenic | X | 38240575 | 38272343 | na | na | criteria provided, single submitter | - |
| Duplication | NM_000531.6(OTC):c.77+2dup | OTC | Likely pathogenic | X | 38212027 | 38212028 | G | GT | criteria provided, single submitter | - |