Variant #0000072969 (NC_000017.10:g.42957940dup, NM_004247.3:c.602dup (EFTUD2))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42957940dup |
DNA change (hg38) |
g.44880572dup |
Published as |
- |
ISCN |
- |
DB-ID |
EFTUD2_000075 |
Variant remarks |
- |
Reference |
PubMed: Vincent et al. |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
De novo |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Dennis E. Bulman |
Database submission license |
No license selected |
Created by |
Dennis E. Bulman |
Date created |
2015-07-02 16:43:45 +02:00 (CEST) |
Date last edited |
2020-07-13 17:02:53 +02:00 (CEST) |

Variant on transcripts
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