Variant #0000223315 (NC_000007.13:g.94257662del, NM_003919.2:c.242del (SGCE))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (paternal) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94257662del |
| DNA change (hg38) |
g.94628350del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SGCE_000058 |
| Variant remarks |
- |
| Reference |
from website {DBsub-Emory} |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Madhuri Hegde |
| Database submission license |
No license selected |
| Created by |
Madhuri Hegde |
| Date created |
2012-10-26 15:21:20 +02:00 (CEST) |
| Date last edited |
2021-07-01 09:21:35 +02:00 (CEST) |

Variant on transcripts
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