Variant #0000782122 (NC_000016.9:g.[(?_2098587)_(2127728_2129032)del;(2137943_2138048)_(2138713_?)del], NC_000016.9(NM_000548.3):c.(?_-29-1)_(2966+1_2967-1)del(;)(5068+1_5069-1)_(*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.[(?_2098587)_(2127728_2129032)del;(2137943_2138048)_(2138713_?)del]
DNA change (hg38) g.[(?_2048586)_(2077727_2079031)del;(2087942_2088047)_(2088712_?)del]
Published as -
ISCN -
DB-ID TSC2_002430 See all 2 reported entries
Variant remarks exons 2-26 and 40-42 deleted
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 2021-05-04 16:22:13 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 +/+ _1i_42_ c.(?_-29-1)_(2966+1_2967-1)del(;)(5068+1_5069-1)_(*102_?)del r.? p.? - -


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