Variant #0000352737 (NC_000017.10:g.7359242_7359250del, NM_000747.2:c.1347_1355del (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.7359242_7359250del |
DNA change (hg38) |
g.7455923_7455931del |
Published as |
- |
ISCN |
- |
DB-ID |
CHRNB1_000003 See all 3 reported entries |
Variant remarks |
expression cloning human CHRNB1 cDNA in HEK293 cells showed 0.30 expression and impaired interaction between beta/delta subunits receptor assembly |
Reference |
PubMed: Quiram 1999 |
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 International |
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) |

Variant on transcripts
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