Variant #0000578201 (NC_000023.10:g.69665044dup, NM_021120.3:c.-8dup (DLG3))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.69665044dup
DNA change (hg38) g.70445194dup
Published as -14_-13insG
ISCN -
DB-ID DLG3_000034 See all 2 reported entries
Variant remarks HEK293T cell expression cloning dual luciferase reporter assay shows reduced protein translation
Reference PubMed: Kumar 2016, Journal: Kumar 2016
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 2019-07-21 13:41:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLG3 NM_021120.3 +/. 1 c.-8dup r.(=) p.(=)


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