Variant #0000597980 (NC_000016.9:g.2108831_2108835del, NM_000548.3:c.932_936del (TSC2))

Chromosome 16
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.2108831_2108835del
DNA change (hg38) g.2058830_2058834del
Published as -
ISCN -
DB-ID TSC2_003593 See all 3 reported entries
Variant remarks 5bp deletion of CTCTC
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site BspCNI-, DdeI-
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 2021-08-18 14:45:40 +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     
TSC2 NM_000548.3 +/+ 10 c.932_936del r.(?) p.(Ser311*) Hamartin binding domain -


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