Variant #0000223326 (NC_000013.10:g.23853468A>G, NC_000013.10(NM_000231.2):c.386-30A>G (SGCG))
| Chromosome |
13 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.23853468A>G |
| DNA change (hg38) |
g.23279329A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SGCG_000060 See all 3 reported entries |
| 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) |
0.09666 View details |
| Owner |
Madhuri Hegde |
| Database submission license |
No license selected |
| Created by |
Madhuri Hegde |
| Date created |
2012-10-26 15:26:18 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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