Variant #0000620071 (NC_000009.11:g.(135804340_135810419)_(135781527_135782117)del, NC_000009.11(NM_000368.4):c.(-81+1_-80-1)_(1438+1_1439-1)del (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.(135804340_135810419)_(135781527_135782117)del
DNA change (hg38) g.(132928953_132935032)_(132906140_132906730)del
Published as -
ISCN -
DB-ID TSC1_001346 See all 2 reported entries
Variant remarks exons 3-14 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 2019-11-15 19:28:56 +01:00 (CET)
Date last edited 2020-06-19 08:46:34 +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     
TSC1 NM_000368.4 +/+ 2i_14i c.(-81+1_-80-1)_(1438+1_1439-1)del r.(?) p.? - -


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