Variant #0000223321 (NC_000013.10:g.23898664G>A, NM_000231.2:c.860G>A (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.23898664G>A |
| DNA change (hg38) |
g.23324525G>A |
| Published as |
860A>G |
| ISCN |
- |
| DB-ID |
SGCG_000037 See all 11 reported entries |
| Variant remarks |
Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message. |
| Reference |
from website {DBsub-Emory} |
| ClinVar ID |
- |
| dbSNP ID |
rs1800354 |
| 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 15:26:18 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
|