Variant #0000684377 (NC_000009.11:g.135772717G>A, NM_000368.4:c.2829C>T (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.135772717G>A
DNA change (hg38) g.132897330G>A
Published as -
ISCN -
DB-ID TSC1_000184 See all 43 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs4962081
Origin SUMMARY record
Segregation -
Frequency 24631/308824 alleles, 1104 homozygotes
Re-site AciI-, HaeIII-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.07947 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2020-08-26 10:25:17 +02:00 (CEST)
Date last edited 2020-11-02 09:57:30 +01:00 (CET)
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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 -/- 22 c.2829C>T r.(?) p.(Ala943=) ERM interaction domain -


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