Variant #0000632416 (NC_000016.9:g.(?_2098587)_(2124391_2125799)del, NC_000016.9(NM_000548.3):c.(?_-29-1)_(2545+1_2546-1)del (TSC2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_2098587)_(2124391_2125799)del |
| DNA change (hg38) |
g.(?_2048586)_(2074390_2075798)del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_002089 See all 2 reported entries |
| Variant remarks |
TSC2 exons 2-22 deleted; found with variant upstream of TSC1 5'UTR c.-1055G>T and TSC2 missense TSC2 c.5359G>A |
| Reference |
unpublished |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| 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 |
2013-02-13 17:56:02 +01:00 (CET) |
| Date last edited |
2021-05-04 16:07:11 +02:00 (CEST) |

Variant on transcripts
Screenings
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