Variant #0000469422 (NC_000009.11:g.135704184_135816758del, NC_000009.11(NM_000368.4):c.-144+3172_*67438del (TSC1))

Chromosome 9
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.135704184_135816758del
DNA change (hg38) g.132828797_132941371del
Published as -
ISCN -
DB-ID TSC1_000488 See all 2 reported entries
Variant remarks 112575bp deletion starting in intron 1 and including exons 2-23 and 3'UTR
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 2019-03-15 13:22:37 +01:00 (CET)
Date last edited 2020-11-02 09:56:34 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC1 NM_000368.4 +/+ 1i_23_ c.-144+3172_*67438del r.? p.? - -


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