Variant #0000067099 (NC_000017.10:g.42962694_42962713del, NC_000017.10(NM_004247.3):c.272-9_282del (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.42962694_42962713del |
| DNA change (hg38) |
g.44885326_44885345del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
EFTUD2_000055 |
| Variant remarks |
- |
| Reference |
Huang et al. 2015 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| 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 |
2015-06-09 17:39:44 +02:00 (CEST) |
| Date last edited |
2020-07-13 17:02:59 +02:00 (CEST) |

Variant on transcripts
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