Variant #0000021463 (NC_000006.11:g.10586465T>A, NC_000006.11(NM_145649.4):c.926-35119T>A (GCNT2))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.10586465T>A |
| DNA change (hg38) |
g.10586232T>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GCNT2_000008 See all 3 reported entries |
| Variant remarks |
expression cloning COS-7 cells, only residual GlcNAc-transferring activity |
| Reference |
PubMed: Lin 2006 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00013 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2013-10-14 23:28:49 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
|