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 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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