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
|