Variant #0000352756 (NC_000017.10:g.4806322C>T, NM_000080.3:c.37G>A (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.4806322C>T |
DNA change (hg38) |
g.4903027C>T |
Published as |
- |
ISCN |
- |
DB-ID |
CHRNE_000005 See all 6 reported entries |
Variant remarks |
expression cloning human cDNA HEK293 cells; reduced expression CHRNE, 0.10 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) |
3.0E-5 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
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) |

Variant on transcripts
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