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_152419.3(HGSNAT):c.1542+1G>A | HGSNAT | Likely pathogenic | 8 | 43052169 | 43052169 | G | A | criteria provided, single submitter | - |
| single nucleotide variant | NM_152419.3(HGSNAT):c.1542+1G>C | HGSNAT | Likely pathogenic | 8 | 43052169 | 43052169 | G | C | criteria provided, single submitter | - |
| single nucleotide variant | NM_152419.3(HGSNAT):c.1614-2A>T | HGSNAT | Likely pathogenic | 8 | 43052981 | 43052981 | A | T | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_152419.3(HGSNAT):c.851+1G>A | HGSNAT | Likely pathogenic | 8 | 43028887 | 43028887 | G | A | criteria provided, single submitter | - |
| single nucleotide variant | NM_152419.3(HGSNAT):c.744-2A>G | HGSNAT | Pathogenic/Likely pathogenic | 8 | 43027451 | 43027451 | A | G | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_152419.3(HGSNAT):c.852-1G>A | HGSNAT | Pathogenic | 8 | 43033216 | 43033216 | G | A | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_152419.3(HGSNAT):c.947G>A (p.Trp316Ter) | HGSNAT | Pathogenic/Likely pathogenic | 8 | 43033312 | 43033312 | G | A | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_152419.3(HGSNAT):c.1031G>A (p.Arg344His) | HGSNAT | Pathogenic/Likely pathogenic | 8 | 43037306 | 43037306 | G | A | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_152419.3(HGSNAT):c.1542+2T>G | HGSNAT | Likely pathogenic | 8 | 43052170 | 43052170 | T | G | criteria provided, single submitter | - |
| single nucleotide variant | NM_152419.3(HGSNAT):c.1674C>G (p.Tyr558Ter) | HGSNAT | Likely pathogenic | 8 | 43053043 | 43053043 | C | G | criteria provided, single submitter | - |