Variant #0000674788 (NC_000016.9:g.2106894_2161281del, NM_000548.3:c.774+124_*102{0} (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.2106894_2161281del |
DNA change (hg38) |
g.2056893_2088712{0} |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_001558 See all 2 reported entries |
Variant remarks |
deletion includes TSC2 exons 9-42 and PKD1 exons 15-46 (PKD1 variant = c.3887_*1017{0}); 54,388bp genomic deletion with breakpoints determined; starts in TSC2 intron 8 (NM_000548.3:c.774+125) and ends in PKD1 exon 15 (NM_000296.3:c.3887) |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
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 |
2020-07-20 14:30:39 +02:00 (CEST) |
Date last edited |
2021-08-18 14:45:40 +02:00 (CEST) |

Variant on transcripts
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