Variant #0000352752 (NC_000002.11:g.233392148T>A, NM_000751.2:c.236T>A (CHRND))

Chromosome 2
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.233392148T>A
DNA change (hg38) g.232527438T>A
Published as I58K
ISCN -
DB-ID CHRND_000010 See all 2 reported entries
Variant remarks expression cloning human cDNA in HEK293; expression reduced to 0.05, complex formation reduced to 0.15
Reference PubMed: Shen 2008, OMIM:var0009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-02-13 11:26:43 +01:00 (CET)
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     
CHRND NM_000751.2 +/. 3 c.236T>A r.(?) p.Ile79Lys


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