Variant #0000782098 (NC_000016.9:g.(?_2097990)_?del(75000), NM_000548.3:c.(?_-106)_?del(75000) (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)_?del(75000)
DNA change (hg38) g.(?_2047989)_?del(75000)
Published as -
ISCN -
DB-ID TSC2_001298 See all 2 reported entries
Variant remarks deletion of ~75kb; part of TSC2 but not PKD1 deleted; adjacent SLC9A3R2 (OCTS2) and NTHL1 (OCTS3) genes also deleted; proximal deletion breakpoint within TSC2 but distal end uncertain
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 2022-06-29 23:30:16 +02:00 (CEST)
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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 +/+ _1_ c.(?_-106)_?del(75000) r.0? p.? - -


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