Variant #0000782068 (NC_000016.9:g.2097981G>T, NM_000548.3:c.-115G>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2097981G>T
DNA change (hg38) g.2047980G>T
Published as -
ISCN -
DB-ID TSC2_002760 See all 2 reported entries
Variant remarks variant is 9 bases 5' of the untranslated exon 1 and is between 2 cETS binding sites in the core promoter region (Kobayashi et al, 1997. DOI: 10.1007/s003359900502)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site MmeI+
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 2021-05-04 16:22:13 +02:00 (CEST)
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     
TSC2 NM_000548.3 -?/-? _1 c.-115G>T r.(?) p.(=) - -


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