Variant #0000945910 (NC_000016.9:g.2136194_2136872{0}, NM_000548.3:c.4663_4989{0} (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.2136194_2136872{0} |
DNA change (hg38) |
g.2086193_2086871{0} |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_001940 See all 2 reported entries |
Variant remarks |
exons 37-38 deleted; breakpoints verified by long-range PCR |
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 |
2023-11-20 13:56:14 +01:00 (CET) |
Date last edited |
N/A |
Variant on transcripts
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