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_000548.5(TSC2):c.2539del (p.Leu847fs) | TSC2 | Pathogenic | 16 | 2124383 | 2124383 | TC | T | criteria provided, single submitter | ClinGen:CA017584,Tuberous sclerosis database (TSC2):TSC2_00776 |
| single nucleotide variant | NM_000548.5(TSC2):c.2661T>A (p.Cys887Ter) | TSC2 | Pathogenic | 16 | 2126090 | 2126090 | T | A | criteria provided, single submitter | ClinGen:CA017829,Tuberous sclerosis database (TSC2):TSC2_00109 |
| Deletion | NM_000548.5(TSC2):c.2733del (p.Phe911fs) | TSC2 | Pathogenic | 16 | 2126162 | 2126162 | TC | T | criteria provided, single submitter | ClinGen:CA017973,Tuberous sclerosis database (TSC2):TSC2_01055 |
| single nucleotide variant | NM_000548.5(TSC2):c.2974C>T (p.Gln992Ter) | TSC2 | Pathogenic | 16 | 2129040 | 2129040 | C | T | criteria provided, single submitter | ClinGen:CA018343,Tuberous sclerosis database (TSC2):TSC2_00137 |
| single nucleotide variant | NM_000548.5(TSC2):c.3094C>T (p.Arg1032Ter) | TSC2 | Pathogenic | 16 | 2129160 | 2129160 | C | T | criteria provided, multiple submitters, no conflicts | Tuberous sclerosis database (TSC2):TSC2_00492,ClinGen:CA018490 |
| single nucleotide variant | NM_000548.5(TSC2):c.3095G>C (p.Arg1032Pro) | TSC2 | Pathogenic/Likely pathogenic | 16 | 2129161 | 2129161 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA018497,Tuberous sclerosis database (TSC2):TSC2_00739 |
| single nucleotide variant | NM_000548.5(TSC2):c.3131+1G>A | TSC2 | Pathogenic | 16 | 2129198 | 2129198 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA018580,Tuberous sclerosis database (TSC2):TSC2_00722 |
| single nucleotide variant | NM_000548.5(TSC2):c.3212C>G (p.Thr1071Arg) | TSC2 | Pathogenic | 16 | 2129357 | 2129357 | C | G | criteria provided, single submitter | ClinGen:CA018689,Tuberous sclerosis database (TSC2):TSC2_00503 |
| Deletion | NM_000548.5(TSC2):c.3310_3311del (p.Gln1104fs) | TSC2 | Pathogenic | 16 | 2129582 | 2129583 | GAC | G | criteria provided, single submitter | ClinGen:CA018864,Tuberous sclerosis database (TSC2):TSC2_01087 |
| single nucleotide variant | NM_000548.5(TSC2):c.3343C>T (p.Gln1115Ter) | TSC2 | Pathogenic | 16 | 2129616 | 2129616 | C | T | criteria provided, single submitter | ClinGen:CA018915,Tuberous sclerosis database (TSC2):TSC2_01059 |