Variant #0000684361 (NC_000016.9:g.(2114429_2115519)_(2124391_2125799)[3], NM_000548.3:c.(1599+1_1600-1)_(2545+1_2546-1)[3] (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.(2114429_2115519)_(2124391_2125799)[3] |
| DNA change (hg38) |
g.(2064428_2065518)_(2074390_2075798)[3] |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_001632 See all 2 reported entries |
| Variant remarks |
triplication of exons 16-22 inclusive resulting in 4 alleles (heterozygous triplication) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Rosemary Ekong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2020-08-26 10:25:17 +02:00 (CEST) |
| Date last edited |
2020-08-27 17:42:33 +02:00 (CEST) |
Variant on transcripts
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