Variant #0000293270 (NC_000016.9:g.2097693C>T, NM_000548.3:c.-403C>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.2097693C>T
DNA change (hg38) g.2047692C>T
Published as NTHL1(NM_002528.7):c.115+17G>A
ISCN -
DB-ID NTHL1_000255
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) 0.00035 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 2022-02-21 16:24:17 +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.-403C>T r.(?) p.(=) - -
PKD1 NM_001009944.2 -/. - c.*42035G>A r.(=) p.(=) - -
NTHL1 NM_002528.5 -/. - c.139+17G>A r.(=) p.(=) - -


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