Variant #0000072973 (NC_000017.10:g.42949875dup, NM_004247.3:c.933dup (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.42949875dup |
| DNA change (hg38) |
g.44872507dup |
| Published as |
- |
| ISCN |
- |
| DB-ID |
EFTUD2_000078 |
| Variant remarks |
- |
| Reference |
PubMed: Sarkar 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 17:33:43 +02:00 (CEST) |
| Date last edited |
2020-07-13 17:02:45 +02:00 (CEST) |

Variant on transcripts
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