Variant #0000518595 (NC_000003.11:g.183858308C>T, NM_003907.2:c.946C>T (EIF2B5))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.183858308C>T |
DNA change (hg38) |
g.184140520C>T |
Published as |
EIF2B5(NM_003907.3):c.946C>T (p.R316*) |
ISCN |
- |
DB-ID |
EIF2B5_000040 |
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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-06-16 09:15:46 +02:00 (CEST) |

Variant on transcripts
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