Variant #0000455941 (NC_000016.9:g.2133726C>T, NM_000548.3:c.3914C>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.2133726C>T
DNA change (hg38) g.2083725C>T
Published as -
ISCN -
DB-ID TSC2_000543 See all 10 reported entries
Variant remarks T389/S6K ratio not significantly different compared to wild type TSC2 but is significantly reduced compared to pathogenic TSC2 p.R611Q; TSC1 and TSC2 signals significantly reduced compared to wild type TSC2; reported that variant did not disrupt TSC2 function
Reference Nellist, personal communication
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00185 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2013-06-12 02:25:54 +02:00 (CEST)
Date last edited 2021-04-23 13:58:39 +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 -/. 33 c.3914C>T - p.Pro1305Leu - -


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