Variant #0000444358 (NC_000004.11:g.?, NM_173660.4:c.? (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.?
DNA change (hg38) -
Published as -
ISCN -
DB-ID DOK7_000000 See all 16 reported entries
Variant remarks expression cloning HEK 293T cells, fails to bind MUSK
Reference PubMed: Hamuro 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-11-28 23:06:23 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOK7 NM_173660.4 +/. 4 c.? - p.Arg159Ala


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