Variant #0000517076 (NC_000002.11:g.88926752_88926754del, NM_004836.5:c.61_63del (EIF2AK3))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88926752_88926754del |
DNA change (hg38) |
g.88627234_88627236del |
Published as |
EIF2AK3(NM_004836.5):c.58_60del (p.(Leu21del)), EIF2AK3(NM_004836.6):c.61_63delCTG (p.L21del), EIF2AK3(NM_004836.7):c.61_63delCTG (p.L21del) |
ISCN |
- |
DB-ID |
EIF2AK3_000024 See all 3 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|