Variant #0000631893 (NC_000002.11:g.88879078_88879079inv, NM_004836.5:c.1843_1844inv (EIF2AK3))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88879078_88879079inv |
| DNA change (hg38) |
g.88579560_88579561inv |
| Published as |
[1843G>T];[1844A>C], 1843_1844delinsTC |
| ISCN |
- |
| DB-ID |
EIF2AK3_000039 |
| Variant remarks |
variant called as c.1843G>T (Asp615Tyr) and c.1844A>C (Asp615Ala) |
| Reference |
Journal: Wakeling 2020 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| 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 14:26:01 +01:00 (CET) |
| Date last edited |
2020-01-23 14:35:41 +01:00 (CET) |

Variant on transcripts
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