Variant #0000780712 (NC_000016.9:g.2115529C>T, NM_000548.3:c.1609C>T (TSC2))

Chromosome 16
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.2115529C>T
DNA change (hg38) g.2065528C>T
Published as -
ISCN -
DB-ID TSC2_002349 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs142257684
Origin SUMMARY record
Segregation -
Frequency 94/316618 alleles
Re-site LpnPI+, AciI-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00014 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2021-05-04 16:22:13 +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     
TSC2 NM_000548.3 -/- 16 c.1609C>T r.(?) p.(Arg537Cys) Hamartin binding domain -


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