Variant #0000443223 (NC_000023.10:g.24521596G>A, PDK3(NM_005391.4):c.473G>A)

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.24521596G>A
DNA change (hg38) g.24503479G>A
Published as -
ISCN -
DB-ID PDK3_000003 See all 4 reported entries
Variant remarks expression cloning, PKD3 hyperactivity (5x increased)
Reference PubMed: Kennerson 2013
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 2013-03-15 18:53:20 +01:00 (CET)
Date last edited 2020-07-17 21:21:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDK3 NM_005391.4 +/. 4 c.473G>A r.(?) p.Arg158His