Variant #0000699529 (NC_000009.11:g.135820786_135820787delinsTT, NM_000368.4:c.-1001_-1000delinsAA (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135820786_135820787delinsTT
DNA change (hg38) g.132945399_132945400delinsTT
Published as -
ISCN -
DB-ID TSC1_000535 See all 2 reported entries
Variant remarks 2bp deletion of GC and 2bp insertion of AA; common variant in 5' upstream region; HGVS nomenclature = NG_012386.1:g.4234_4235delinsAA
Reference -
ClinVar ID -
dbSNP ID rs386739091
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 2020-11-02 10:52:17 +01:00 (CET)
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     
TSC1 NM_000368.4 -/- _1 c.-1001_-1000delinsAA r.(?) p.(=) - -


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