Variant #0000684084 (NC_000016.9:g.2138319_2138345del, NC_000016.9(NM_000548.3):c.5252_5259+19del (TSC2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2138319_2138345del |
| DNA change (hg38) |
g.2088318_2088344del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_000661 See all 26 reported entries |
| Variant remarks |
27bp deletion (GCCAGCGGgtagggaatatggggctcc) includes ex41 and intron 41; 100 nt. of intron 41 inserted (ctcagcggggtgtgctggctgcccaagctgtggggcgggtgtgtgggcagagcggttgccacgcctcccagacttactgcccaagccgcctctgccttca) creating 34 new aa (RNA evidence) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
BanII-, EciI- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Rosemary Ekong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2020-08-26 09:13:20 +02:00 (CEST) |
| Date last edited |
2021-08-18 14:47:59 +02:00 (CEST) |

Variant on transcripts
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