Variant #0000223341 (NC_000013.10:g.23768928G>A, NC_000013.10(NM_000231.2):c.1-8906G>A (SGCG))
| Chromosome |
13 |
| Allele |
Parent #1 |
| 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.23768928G>A |
| DNA change (hg38) |
g.23194789G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SGCG_000016 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs3794367 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.51 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2005-01-15 14:57:07 +01:00 (CET) |
| Date last edited |
2012-11-02 20:43:04 +01:00 (CET) |

Variant on transcripts
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