Variant #0000780223 (NC_000016.9:g.2098629A>G, NM_000548.3:c.13A>G (TSC2))

Chromosome 16
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.2098629A>G
DNA change (hg38) g.2048628A>G
Published as -
ISCN -
DB-ID TSC2_000932 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs45517093
Origin SUMMARY record
Segregation -
Frequency 1/263920 alleles
Re-site Cac8I+, MwoI+
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 2021-05-04 16:22:13 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 -?/-? 2 c.13A>G r.(?) p.(Thr5Ala) Hamartin binding domain -


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