Variant #0000469588 (NC_000009.11:g.135786839C>T, NC_000009.11(NM_000368.4):c.1029+1G>A (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.135786839C>T
DNA change (hg38) g.132911452C>T
Published as -
ISCN -
DB-ID TSC1_000062 See all 9 reported entries
Variant remarks donor splice site affected; retention of intron 10 results in the addition of 113 amino acids
Reference -
ClinVar ID -
dbSNP ID rs118203485
Origin SUMMARY record
Segregation -
Frequency 1/251294 alleles
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2019-03-15 13:22:37 +01:00 (CET)
Date last edited 2020-11-02 09:57:30 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC1 NM_000368.4 +/+ 10i c.1029+1G>A r.[=, 1029_1030ins1029+1_1030-1] p.[=, Gln343_Ala344insVal*24] Tuberin binding domain affects splicing


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.