Variant #0000352725 (NC_000002.11:g.175618298G>C, NM_001039523.2:c.786C>G (CHRNA1))

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.175618298G>C
DNA change (hg38) g.174753570G>C
Published as C651G (N217K)
ISCN -
DB-ID CHRNA1_000002 See all 2 reported entries
Variant remarks expression cloning mouse CHRNA1 cDNA in HEK293 cells showed prolonged channel open intervals/bursts, increased affinity for ACh, enhanced desensitization
Reference PubMed: Engel 1996
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 11:22:31 +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     
CHRNA1 NM_001039523.2 +/. 7 c.786C>G r.(?) p.Asn262Lys


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