Variant #0000352753 (NC_000002.11:g.233394841C>A, NM_000751.2:c.812C>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.233394841C>A
DNA change (hg38) g.232530131C>A
Published as P250Q
ISCN -
DB-ID CHRND_000011 See all 8 reported entries
Variant remarks expression cloning human CHRND cDNA in HEK293 cells shows reduced AChR assembly, hinders opening doubly occupied closed receptor, speeded dissociation acetylcholine from A2R (fast channel effects)
Reference PubMed: Shen 2002, OMIM:var0002
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 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 +/. 7 c.812C>A r.(?) p.Pro271Gln


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