Variant #0000223261 (NC_000017.10:g.48244683G>C, NC_000017.10(NM_000023.2):c.38-46G>C (SGCA))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48244683G>C |
| DNA change (hg38) |
g.50167322G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SGCA_000113 |
| Variant remarks |
- |
| Reference |
from website {DBsub-Emory} |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00894 View details |
| Owner |
Madhuri Hegde |
| Database submission license |
No license selected |
| Created by |
Madhuri Hegde |
| Date created |
2012-10-26 15:17:26 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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