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) | ||||||||||
| Duplication | NM_000321.3(RB1):c.19dup (p.Arg7fs) | RB1 | Pathogenic | 13 | 48878061 | 48878062 | A | AC | criteria provided, multiple submitters, no conflicts | ClinGen:CA609859297 |
| Duplication | NM_000321.3(RB1):c.54_76dup (p.Pro26fs) | RB1 | Pathogenic/Likely pathogenic | 13 | 48878093 | 48878094 | T | TGCCGCCGCGGAACCCCCGGCACC | criteria provided, multiple submitters, no conflicts | ClinGen:CA645369601 |
| Deletion | NM_000321.3(RB1):c.106del (p.Asp36fs) | RB1 | Pathogenic | 13 | 48878153 | 48878153 | AG | A | criteria provided, single submitter | ClinGen:CA645369602 |
| single nucleotide variant | NM_000321.3(RB1):c.137+1G>T | RB1 | Pathogenic | 13 | 48878186 | 48878186 | G | T | criteria provided, single submitter | ClinGen:CA388250409 |
| single nucleotide variant | NM_000321.3(RB1):c.264+1G>A | RB1 | Pathogenic | 13 | 48881543 | 48881543 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA388250701 |
| single nucleotide variant | NM_000321.3(RB1):c.277C>T (p.Gln93Ter) | RB1 | Pathogenic/Likely pathogenic | 13 | 48916747 | 48916747 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA388252335 |
| Duplication | NM_000321.3(RB1):c.281dup (p.Lys95fs) | RB1 | Pathogenic | 13 | 48916747 | 48916748 | C | CA | criteria provided, single submitter | ClinGen:CA645369550 |
| single nucleotide variant | NM_000321.3(RB1):c.380G>A (p.Ser127Asn) | RB1 | Likely pathogenic | 13 | 48916850 | 48916850 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA388252575 |
| single nucleotide variant | NM_000321.3(RB1):c.380G>C (p.Ser127Thr) | RB1 | Likely pathogenic | 13 | 48916850 | 48916850 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA388252576 |
| single nucleotide variant | NM_000321.3(RB1):c.380+1G>A | RB1 | Pathogenic | 13 | 48916851 | 48916851 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA388252578 |