Variant #0000631894 (NC_000002.11:g.88879079C>A, NM_004836.5:c.1843G>T (EIF2AK3))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88879079C>A |
| DNA change (hg38) |
g.88579561C>A |
| Published as |
[1843G>T];[1844A>C] |
| ISCN |
- |
| DB-ID |
EIF2AK3_000040 |
| Variant remarks |
correct is two flanking variants on one allele (c.1843_1844inv) |
| Reference |
Journal: Wakeling 2020 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Artefact |
| 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 |
2020-01-23 14:28:43 +01:00 (CET) |
| Date last edited |
2020-07-14 22:03:31 +02:00 (CEST) |

Variant on transcripts
|