Variant #0000469568 (NC_000009.11:g.?, NM_000368.4:c.[-234-u5895_-144+825del;chr9:g.135822115_135822270inv] (TSC1))

Chromosome 9
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.?
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC1_000485 See all 2 reported entries
Variant remarks 6811bp deletion; variant includes exon 1, upstream region, and a 156bp inverted sequence upstream of exon 1; promoter region reported between nts. -157bp and -744bp completely deleted
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 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2019-03-15 13:22:37 +01:00 (CET)
Date last edited 2020-11-02 09:56:34 +01:00 (CET)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC1 NM_000368.4 +?/+? _1_1i c.[-234-u5895_-144+825del;chr9:g.135822115_135822270inv] r.0? p.0? - -


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