Variant #0000782301 (NC_000016.9:g.2098578G>C, NC_000016.9(NM_000548.3):c.-29-10G>C (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.2098578G>C
DNA change (hg38) g.2048577G>C
Published as -
ISCN -
DB-ID TSC2_003022 See all 7 reported entries
Variant remarks variant in intron 1
Reference -
ClinVar ID -
dbSNP ID rs28537973
Origin SUMMARY record
Segregation -
Frequency 505/304440 alleles, 4 homozygotes
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00075 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 -/- 1i c.-29-10G>C r.(?) p.(=) - -


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