Variant #0000782305 (NC_000016.9:g.2098586_2098741del, NC_000016.9(NM_000548.3):c.-29-2_125del (TSC2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2098586_2098741del |
| DNA change (hg38) |
g.2048585_2048740del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_001095 |
| Variant remarks |
part of exon 2 deleted; 156bp genomic deletion starting in intron 1 and involving first 42 codons of exon 2 (including the start codon); splice site affected |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
AciI-, FatI- |
| 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 |
2021-05-04 16:22:13 +02:00 (CEST) |
| Date last edited |
2021-05-06 00:06:30 +02:00 (CEST) |

Variant on transcripts
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