Variant #0000352758 (NC_000017.10:g.4805239G>A, NM_000080.3:c.488C>T (CHRNE))

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.4805239G>A
DNA change (hg38) g.4901944G>A
Published as -
ISCN -
DB-ID CHRNE_000007 See all 6 reported entries
Variant remarks expression cloning human cDNA HEK293 cells; reduced expression CHRNE, reduced assembly with other subunits, no assembly with CHRNA
Reference PubMed: Ohno 1996
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00027 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 2011-12-29 17:55:05 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRNE NM_000080.3 +/. 5 c.488C>T r.(?) p.Ser163Leu


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.