Variant #0000557337 (NC_000016.9:g.2142146del, NM_000548.3:c.*3535del (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2142146del
DNA change (hg38) g.2092145del
Published as -
ISCN -
DB-ID PKD1_002881
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) Retrieve
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 2022-02-21 16:37:10 +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.*3535del r.(?) p.(=) - -
PKD1 NM_001009944.2 +/. - c.11314del r.(?) p.(Ala3772ProfsTer54) - -
NTHL1 NM_002528.5 +/. - c.-44297del r.(?) p.(=) - -


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