Variant #0000444372 (NC_000004.11:g.3465269C>A, NM_173660.4:c.91C>A (DOK7))

Chromosome 4
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.3465269C>A
DNA change (hg38) g.3463542C>A
Published as -
ISCN -
DB-ID DOK7_000060 See all 2 reported entries
Variant remarks expression cloning differentiated C2C12 cells, significantly reduced AChR clustering, reduced complexity
Reference PubMed: Cossins 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 2012-07-08 11:53:08 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOK7 NM_173660.4 +/. 2 c.91C>A r.(?) p.Pro31Thr


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