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_138694.4(PKHD1):c.11074C>T (p.Arg3692Ter) | PKHD1 | Pathogenic/Likely pathogenic | 6 | 51523850 | 51523850 | G | A | criteria provided, multiple submitters, no conflicts | - |
| Deletion | NM_138694.4(PKHD1):c.383del (p.Thr128fs) | PKHD1 | Pathogenic | 6 | 51944705 | 51944705 | AG | A | criteria provided, multiple submitters, no conflicts | - |
| Duplication | NM_138694.4(PKHD1):c.4118dup (p.Met1373fs) | PKHD1 | Pathogenic/Likely pathogenic | 6 | 51890489 | 51890490 | C | CA | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_138694.4(PKHD1):c.11747C>G (p.Ser3916Ter) | PKHD1 | Pathogenic/Likely pathogenic | 6 | 51491833 | 51491833 | G | C | criteria provided, multiple submitters, no conflicts | - |
| Indel | NM_138694.4(PKHD1):c.6866-2_6866-1delinsGA | PKHD1 | Pathogenic/Likely pathogenic | 6 | 51768526 | 51768527 | CT | TC | criteria provided, multiple submitters, no conflicts | - |
| Duplication | NM_001009944.3(PKD1):c.10092dup (p.Leu3365fs) | PKD1 | Pathogenic | 16 | 2147943 | 2147944 | G | GC | criteria provided, single submitter | - |
| single nucleotide variant | NM_001009944.3(PKD1):c.8873C>A (p.Ser2958Ter) | PKD1 | Pathogenic | 16 | 2152890 | 2152890 | G | T | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_000297.4(PKD2):c.2407C>T (p.Arg803Ter) | PKD2 | Pathogenic | 4 | 88989098 | 88989098 | C | T | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_001009944.3(PKD1):c.12724C>T (p.Gln4242Ter) | PKD1 | Likely pathogenic | 16 | 2139916 | 2139916 | G | A | criteria provided, multiple submitters, no conflicts | - |
| Deletion | NM_001009944.3(PKD1):c.12592_12619del (p.Ser4198fs) | PKD1 | Likely pathogenic | 16 | 2140021 | 2140048 | CTTGTCCCCAGCCGGCCCAGGCTCACGCT | C | criteria provided, single submitter | - |