Variant #0000021460 (NC_000006.11:g.10626680G>A, NM_145649.4:c.1049G>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.10626680G>A |
| DNA change (hg38) |
g.10626447G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GCNT2_000001 See all 12 reported entries |
| Variant remarks |
expression cloning CHO cells, no I-antigen expression |
| Reference |
PubMed: Inaba 2003 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
5.0E-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 |
2013-10-14 23:02:57 +02:00 (CEST) |
| Date last edited |
2024-01-31 16:47:39 +01:00 (CET) |

Variant on transcripts
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