Variant #0000709327 (NC_000016.9:g.2138100A>G, NM_000548.3:c.5120A>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.2138100A>G
DNA change (hg38) g.2088099A>G
Published as -
ISCN -
DB-ID TSC2_002643 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs772439098
Origin SUMMARY record
Segregation -
Frequency 6/202004 alleles
Re-site ApeKI+, BfuAI-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2020-12-24 09:47:49 +01:00 (CET)
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 -?/-? 40 c.5120A>G r.(?) p.(Asn1707Ser) GAP domain -


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