Variant #0000309667 (NC_000016.9:g.2134994C>T, NM_000548.3:c.4536C>T (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.2134994C>T
DNA change (hg38) g.2084993C>T
Published as TSC2(NM_000548.3):c.4536C>T (p.D1512=, p.(Asp1512=)), TSC2(NM_000548.5):c.4536C>T (p.D1512=), TSC2(NM_001114382.2):c.4467C>T (p.D1489=)
ISCN -
DB-ID TSC2_000018 See all 16 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00313 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 -/. - c.4536C>T r.(?) p.(Asp1512=) - -
PKD1 NM_001009944.2 -/. - c.*4734G>A r.(=) p.(=) - -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.