Variant #0000674788 (NC_000016.9:g.2106894_2161281del, NM_000548.3:c.774+124_*102{0} (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.2106894_2161281del
DNA change (hg38) g.2056893_2088712{0}
Published as -
ISCN -
DB-ID TSC2_001558 See all 2 reported entries
Variant remarks deletion includes TSC2 exons 9-42 and PKD1 exons 15-46 (PKD1 variant = c.3887_*1017{0}); 54,388bp genomic deletion with breakpoints determined; starts in TSC2 intron 8 (NM_000548.3:c.774+125) and ends in PKD1 exon 15 (NM_000296.3:c.3887)
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 2020-07-20 14:30:39 +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 +/+ 8i_42_ c.774+124_*102{0} r.? p.? - -
PKD1 NM_001009944.2 +/. - c.3887_*1017{0} r.? p.? - -


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