Variant #0000444381 (NC_000004.11:g.3475262C>T, NM_173660.4:c.230C>T (DOK7))
| Chromosome |
4 |
| 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.3475262C>T |
| DNA change (hg38) |
g.3473535C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
DOK7_000062 See all 2 reported entries |
| Variant remarks |
expression cloning differentiated C2C12 cells, non-significantly reduced AChR clustering (0.5), reduced complexity |
| Reference |
PubMed: Cossins 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-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 |
2012-07-08 11:53:08 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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