Variant #0000352733 (NC_000017.10:g.?, NM_000747.2:c.? (CHRNB1))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CHRNB1_000000 See all 14 reported entries |
| Variant remarks |
expression cloning human CHRNB1 cDNA in HEK293 cells showed normal AChR 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) |
Genomic location of variant could not be determined |
| 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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