Variant #0000699612 (NC_000009.11:g.(135779842_135780967)_(135781527_135782117)del, NC_000009.11(NM_000368.4):c.(1438+1_1439-1)_(1997+1_1998-1)del (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
DNA change (genomic) (Relative to hg19 / GRCh37) g.(135779842_135780967)_(135781527_135782117)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC1_001378 See all 2 reported entries
Variant remarks exon 15 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 2020-11-02 10:52:17 +01:00 (CET)
Date last edited N/A
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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 +?/+? 14i_15i c.(1438+1_1439-1)_(1997+1_1998-1)del r.? p.? - -


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