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_000546.6(TP53):c.375G>C (p.Thr125=) | TP53 | Pathogenic | 17 | 7579312 | 7579312 | C | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA497926317 |
| Deletion | NM_000546.6(TP53):c.310_329del (p.Gln104fs) | TP53 | Pathogenic | 17 | 7579358 | 7579377 | ACGGAAACCGTAGCTGCCCTG | A | criteria provided, single submitter | ClinGen:CA658656635 |
| Duplication | NM_000546.6(TP53):c.121_124dup (p.Asp42delinsGlyTer) | TP53 | Pathogenic | 17 | 7579562 | 7579563 | T | TCATC | criteria provided, single submitter | ClinGen:CA658656662 |
| single nucleotide variant | NM_000546.6(TP53):c.994-2A>G | TP53 | Pathogenic | 17 | 7574035 | 7574035 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA287485766 |
| single nucleotide variant | NM_000546.6(TP53):c.920-1G>T | TP53 | Pathogenic | 17 | 7576927 | 7576927 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA397836174 |
| Insertion | NM_000546.6(TP53):c.842_843insG (p.Asp281fs) | TP53 | Pathogenic | 17 | 7577095 | 7577096 | G | GC | criteria provided, single submitter | ClinGen:CA658656538 |
| single nucleotide variant | NM_000546.6(TP53):c.772G>T (p.Glu258Ter) | TP53 | Pathogenic | 17 | 7577509 | 7577509 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA397837685 |
| single nucleotide variant | NM_000546.6(TP53):c.532C>G (p.His178Asp) | TP53 | Likely pathogenic | 17 | 7578398 | 7578398 | G | C | reviewed by expert panel | ClinGen:CA397841387 |
| Deletion | NM_000546.6(TP53):c.509_512del (p.Thr170fs) | TP53 | Pathogenic | 17 | 7578418 | 7578421 | CTCCG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656581 |
| Duplication | NM_000546.6(TP53):c.38dup (p.Leu14fs) | TP53 | Pathogenic/Likely pathogenic | 17 | 7579874 | 7579875 | A | AG | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656673 |