Variant #0001047190 (NC_000016.9:g.2136455C>T, NC_000016.9(NM_000548.3):c.4849+75C>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2136455C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC2_002646 See all 11 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs76029733
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-06 16:38:01 +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 -?/. - c.4849+75C>T r.(?) p.(?) - -


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