Variant #0000352736 (NC_000017.10:g.7357660G>A, NM_000747.2:c.865G>A (CHRNB1))

Chromosome 17
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.7357660G>A
DNA change (hg38) g.7454341G>A
Published as G796A (V266M)
ISCN -
DB-ID CHRNB1_000002 See all 4 reported entries
Variant remarks expression cloning mouse CHRNB1 cDNA in HEK293 cells showed prolonged channel open intervals/bursts and spontaneous channel openings, increased affinity for ACh
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 11:25:00 +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     
CHRNB1 NM_000747.2 +/. 8 c.865G>A r.865g>a p.Val289Met


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