Variant #0000989998 (NC_000016.9:g.?, NM_000548.3:c.? (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.? |
DNA change (hg38) |
g.? |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_003425 See all 2 reported entries |
Variant remarks |
5 other variants in the database that result in the generation of r.976_1119del are classified as pathogenic |
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 |
2024-08-21 22:51:56 +02:00 (CEST) |
Date last edited |
2024-08-21 23:13:25 +02:00 (CEST) |
Variant on transcripts
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