Variant #0000632375 (NC_000016.9:g.2137899G>A, NM_000548.3:c.5025G>A (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2137899G>A
DNA change (hg38) g.2087898G>A
Published as -
ISCN -
DB-ID TSC2_000630 See all 9 reported entries
Variant remarks found with TSC2 splice variant (not specified) and TSC1 silent variant c.3324C>T; both TSC1 and TSC2 genes tested
Reference unpublished
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site BsrI+, AciI-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00104 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2011-02-25 21:41:52 +01:00 (CET)
Date last edited 2021-04-23 13:58:39 +02:00 (CEST)
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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 -/. 39 c.5025G>A r.(?) p.(Pro1675=) GAP domain -



Screenings

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