Variant #0000984940 (NC_000016.9:g.(?_2098587)_(2114429_2115519)dup, NC_000016.9(NM_000548.3):c.(?_-29-1)_(1599+1_1600-1)dup (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.(?_2098587)_(2114429_2115519)dup
DNA change (hg38) g.(?_2048586)_(2064428_2065518)dup
Published as -
ISCN -
DB-ID TSC2_001968 See all 2 reported entries
Variant remarks exons 2-15 duplicated
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 2024-04-24 22:30:46 +02:00 (CEST)
Date last edited 2024-06-21 02:07:32 +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 +?/+? _1i_15i c.(?_-29-1)_(1599+1_1600-1)dup r.? p.? - -


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