Variant #0000597996 (NC_000009.11:g.(?_135766735)_?del(147000), NM_000368.4:c.(?_-234)_?del(147000) (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_135766735)_?del(147000)
DNA change (hg38) g.(?_132891348)_?del(147000)
Published as -
ISCN -
DB-ID TSC1_001345 See all 2 reported entries
Variant remarks 147kb deletion involving part of TSC1, GF11B and GTF3C5 (both genes at 5’ of TSC1); deletedTSC1 exons not mentioned and extent of deletion into TSC1 undetermined
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 2019-10-11 19:09:07 +02:00 (CEST)
Date last edited 2022-08-17 17:24:06 +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 ?/? _1 c.(?_-234)_?del(147000) r.0? p.0? - -


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