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_000138.4(FBN1):c.6497_6616del | FBN1 | Pathogenic | 15 | 48726791 | 48726910 | CCTTCACATGTCATCATTGGACCGGGCTCAAATCCCTCCTCGCAGGTGCATTCAAAACCTCCAATCACATTCTTGCAGGTTCCATTTCCACAAGGATTGCCAACAGAACATTCATCAGTAT | C | criteria provided, single submitter | - |
| Deletion | NM_000138.4(FBN1):c.6038_6163del | FBN1 | Pathogenic | 15 | 48733918 | 48734043 | CCTTGGCACCTTCTTCCACTGGAGGACAAGGAAAACCCTTCTGGACACAGACATTTGAAGCTGCCTTCAGTGTTACTGCATGTGCCCAGGGCACAAATTTCTGGCTCTTCGACACACTCATCAATAT | C | criteria provided, single submitter | - |
| Deletion | NM_000138.4(FBN1):c.5225_5296del | FBN1 | Pathogenic | 15 | 48752443 | 48752514 | CCAACGGGTAAACCGGTATAAATGTCGATGACAAAGCCTGGCCTTTGACTTCCACAGAGTGTAGCAAACTCAT | C | criteria provided, single submitter | - |
| Deletion | NM_000138.5(FBN1):c.1659del (p.His554fs) | FBN1 | Pathogenic | 15 | 48802296 | 48802296 | GA | G | criteria provided, single submitter | - |
| Deletion | NC_000015.10:g.(?_48460226)_(48460337_?)del | FBN1 | Pathogenic | 15 | 48752423 | 48752534 | na | na | criteria provided, single submitter | - |
| Duplication | NC_000015.9:g.(?_48888460)_(48905309_?)dup | FBN1 | Likely pathogenic | 15 | 48888460 | 48905309 | na | na | criteria provided, single submitter | - |
| single nucleotide variant | NM_000138.5(FBN1):c.8056T>C (p.Cys2686Arg) | FBN1 | Pathogenic | 15 | 48704936 | 48704936 | A | G | criteria provided, single submitter | - |
| single nucleotide variant | NM_000138.5(FBN1):c.7987T>C (p.Cys2663Arg) | FBN1 | Pathogenic | 15 | 48707797 | 48707797 | A | G | criteria provided, single submitter | - |
| single nucleotide variant | NM_000138.5(FBN1):c.7664G>T (p.Gly2555Val) | FBN1 | Pathogenic | 15 | 48713790 | 48713790 | C | A | criteria provided, multiple submitters, no conflicts | - |
| single nucleotide variant | NM_000138.5(FBN1):c.7279T>C (p.Cys2427Arg) | FBN1 | Likely pathogenic | 15 | 48717987 | 48717987 | A | G | criteria provided, single submitter | - |