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_000053.4(ATP7B):c.1063C>T (p.Gln355Ter) | ATP7B | Pathogenic/Likely pathogenic | 13 | 52548293 | 52548293 | G | A | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_000053.4(ATP7B):c.994G>T (p.Glu332Ter) | ATP7B | Pathogenic | 13 | 52548362 | 52548362 | C | A | criteria provided, multiple submitters, no conflicts | - |
| Duplication | NM_000053.4(ATP7B):c.111dup (p.Ala38fs) | ATP7B | Pathogenic | 13 | 52549244 | 52549245 | C | CA | criteria provided, multiple submitters, no conflicts | - |
| Duplication | NM_000053.4(ATP7B):c.4283dup (p.Ser1429fs) | ATP7B | Pathogenic/Likely pathogenic | 13 | 52509006 | 52509007 | C | CA | criteria provided, multiple submitters, no conflicts | - |
| Deletion | NM_000053.4(ATP7B):c.4006del (p.Ile1336fs) | ATP7B | Pathogenic | 13 | 52511427 | 52511427 | AT | A | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_000053.4(ATP7B):c.3800A>C (p.Asp1267Ala) | ATP7B | Likely pathogenic | 13 | 52511715 | 52511715 | T | G | criteria provided, single submitter | - |
| single nucleotide variant | NM_000053.4(ATP7B):c.3436G>A (p.Val1146Met) | ATP7B | Likely pathogenic | 13 | 52515337 | 52515337 | C | T | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_000053.4(ATP7B):c.3190G>A (p.Glu1064Lys) | ATP7B | Pathogenic/Likely pathogenic | 13 | 52518298 | 52518298 | C | T | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_000053.4(ATP7B):c.3128T>C (p.Leu1043Pro) | ATP7B | Likely pathogenic | 13 | 52518360 | 52518360 | A | G | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_000053.4(ATP7B):c.3086C>T (p.Thr1029Ile) | ATP7B | Pathogenic/Likely pathogenic | 13 | 52518402 | 52518402 | G | A | criteria provided, multiple submitters, no conflicts | - |