Variant #0000598102 (NC_000016.9:g.(?_2097990)_(2138713_?)del, NM_000548.3:c.(?_-106)_(*102_?)del (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.(?_2097990)_(2138713_?)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC2_003687 See all 19 reported entries
Variant remarks complete deletion of TSC2 gene + PKD1 exons 20-46
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 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2019-10-12 13:59:45 +02:00 (CEST)
Date last edited 2021-08-18 14:44:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 +/+ _1_42_ c.(?_-106)_(*102_?)del r.0? p.0? - -


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