Variant #0000557338 (NC_000016.9:g.2142501C>T, NM_000548.3:c.*3890C>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2142501C>T
DNA change (hg38) g.2092500C>T
Published as PKD1(NM_000296.3):c.11246G>A (p.(Arg3749Gln))
ISCN -
DB-ID PKD1_000466 See all 4 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 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 ?/. - c.*3890C>T r.(=) p.(=) - -
PKD1 NM_001009944.2 ?/. - c.11249G>A r.(?) p.(Arg3750Gln) - -
NTHL1 NM_002528.5 ?/. - c.-44653G>A r.(?) p.(=) - -


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