Variant #0000684379 (NC_000009.11:g.135802555C>T, NC_000009.11(NM_000368.4):c.210+33G>A (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.135802555C>T
DNA change (hg38) g.132927168C>T
Published as -
ISCN -
DB-ID TSC1_000008 See all 10 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs118203350
Origin SUMMARY record
Segregation -
Frequency 2754/302544 alleles in 17 populations, 27 homozygotes in 6 populations
Re-site NdeI-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00946 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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC1 NM_000368.4 -/- 4i c.210+33G>A r.(?) p.(=) - -


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