Variant #0000456164 (NC_000009.11:g.135786954C>T, NM_000368.4:c.915G>A (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.135786954C>T
DNA change (hg38) g.132911567C>T
Published as -
ISCN -
DB-ID TSC1_000682 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs397515293
Origin SUMMARY record
Segregation -
Frequency 5/131088 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 2019-02-14 10:55:34 +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 -?/-? 10 c.915G>A r.(?) p.(Gly305=) Tuberin binding domain -


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