Variant #0000067102 (NC_000017.10:g.42956919C>T, NC_000017.10(NM_004247.3):c.702+5G>A (EFTUD2))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42956919C>T |
| DNA change (hg38) |
g.44879551C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
EFTUD2_000058 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
Huang et al. 2015 |
| 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 |
2015-06-09 18:00:12 +02:00 (CEST) |
| Date last edited |
2020-07-13 17:02:50 +02:00 (CEST) |

Variant on transcripts
|