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) | ||||||||||
| Deletion | NM_000546.6(TP53):c.445del (p.Ser149fs) | TP53 | Pathogenic | 17 | 7578485 | 7578485 | GA | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA16620632 |
| Deletion | NM_000546.6(TP53):c.327_328del (p.Phe109fs) | TP53 | Pathogenic/Likely pathogenic | 17 | 7579359 | 7579360 | CGG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA16620636 |
| Deletion | NM_000546.6(TP53):c.273_279del (p.Trp91fs) | TP53 | Pathogenic/Likely pathogenic | 17 | 7579408 | 7579414 | ACAGGGGC | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16620638 |
| Deletion | NM_000546.6(TP53):c.254del (p.Pro85fs) | TP53 | Pathogenic | 17 | 7579433 | 7579433 | AG | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16620639 |
| single nucleotide variant | NM_000546.6(TP53):c.159G>A (p.Trp53Ter) | TP53 | Pathogenic | 17 | 7579528 | 7579528 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16620640 |
| Deletion | NM_000546.6(TP53):c.1049_1050del (p.Leu350fs) | TP53 | Pathogenic | 17 | 7573977 | 7573978 | TGA | T | criteria provided, single submitter | ClinGen:CA645369694 |
| Deletion | NM_000546.6(TP53):c.1024del (p.Arg342fs) | TP53 | Pathogenic | 17 | 7574003 | 7574003 | CG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA497712605 |
| Deletion | NM_000546.6(TP53):c.1018del (p.Met340fs) | TP53 | Pathogenic | 17 | 7574009 | 7574009 | AT | A | criteria provided, single submitter | ClinGen:CA645369695 |
| single nucleotide variant | NM_000546.6(TP53):c.1000G>T (p.Gly334Trp) | TP53 | Likely pathogenic | 17 | 7574027 | 7574027 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA397832878 |
| Deletion | NM_000546.6(TP53):c.993+1del | TP53 | Pathogenic | 17 | 7576852 | 7576852 | AC | A | reviewed by expert panel | ClinGen:CA645369685 |