Variant #0000352741 (NC_000002.11:g.?, NM_000751.2:c.? (CHRND))

Chromosome 2
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.?
DNA change (hg38) -
Published as K382E
ISCN -
DB-ID CHRND_000000 See all 8 reported entries
Variant remarks expression cloning in mouse cDNA HEK293 cells, co-transfected RPASN slightly reduced cluster formation
Reference PubMed: Muller 2006
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 Angela Abicht
Database submission license No license selected
Created by Angela Abicht
Date created 2011-02-13 11:26:43 +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     
CHRND NM_000751.2 +?/. 10 c.? - p.Lys403Glu


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