Variant #0000699505 (NC_000009.11:g.135782202C>G, NM_000368.4:c.1354G>C (TSC1))

Chromosome 9
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.135782202C>G
DNA change (hg38) g.132906815C>G
Published as -
ISCN -
DB-ID TSC1_000340 See all 5 reported entries
Variant remarks Combination of p.Gly452Arg (c.1354G>C) + p.Lys745Met (c.2234A>T) tested; reported that the double mutant did not disrupt TSC2 function in vitro
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Mark Nellist
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 -?/-? 14 c.1354G>C r.(?) p.(Gly452Arg) Tuberin binding domain -


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