Variant #0000945910 (NC_000016.9:g.2136194_2136872{0}, NM_000548.3:c.4663_4989{0} (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.2136194_2136872{0}
DNA change (hg38) g.2086193_2086871{0}
Published as -
ISCN -
DB-ID TSC2_001940 See all 2 reported entries
Variant remarks exons 37-38 deleted; breakpoints verified by long-range PCR
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2023-11-20 13:56:14 +01:00 (CET)
Date last edited N/A




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 +?/+? 37_38 c.4663_4989{0} r.(?) p.(Ser1555_Lys1663del) GAP domain -


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