Variant #0000864421 (NC_000016.9:g.2142143G>C, NM_000548.3:c.*3532G>C (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.2142143G>C
DNA change (hg38) -
Published as PKD1(NM_000296.3):c.11313C>G (p.(Ala3771=)), PKD1(NM_001009944.2):c.11316C>G (p.A3772=)
ISCN -
DB-ID NTHL1_000301 See all 2 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) 0.00149 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +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.*3532G>C r.(=) p.(=) - -
PKD1 NM_001009944.2 -?/. - c.11316C>G r.(?) p.(Ala3772=) - -
NTHL1 NM_002528.5 -?/. - c.-44295C>G r.(?) p.(=) - -


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