Variant #0000918085 (NC_000016.9:g.2122982C>T, NM_000548.3:c.2353C>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2122982C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC2_000708 See all 12 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs45517226
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 2023-01-29 18:52:01 +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 +/. - c.2353C>T r.(?) p.(Gln785Ter) - -


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