Variant #0000444354 (NC_000004.11:g.3465276C>T, NM_173660.4:c.98C>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.3465276C>T |
DNA change (hg38) |
g.3463549C>T |
Published as |
- |
ISCN |
- |
DB-ID |
DOK7_000025 See all 3 reported entries |
Variant remarks |
expression cloning, fails to induce MUSK (Tyr phosphorylation) |
Reference |
PubMed: Hamuro 2008 |
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 |
2011-11-28 23:06:23 +01:00 (CET) |
Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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