Variant #0000815698 (NC_000008.10:g.42698200C>T, NM_018105.2:c.38G>A (THAP1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.42698200C>T
DNA change (hg38) g.42843057C>T
Published as -
ISCN -
DB-ID THAP1_000051 See all 2 reported entries
Variant remarks luciferase reporter gene assay 0.8 THAP1 activity
Reference PubMed: Lohmann 2012
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-10-21 11:51:48 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THAP1 NM_018105.2 +?/. - c.38G>A - p.Arg13His


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