Variant #0000876499 (NC_000011.9:g.45832509A>G, NM_018389.4:c.718A>G (SLC35C1))
| Chromosome |
11 |
| 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.45832509A>G |
| DNA change (hg38) |
g.45810958A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SLC35C1_000031 |
| Variant remarks |
corrected after consultation authors |
| Reference |
PubMed: van de Vijver 2012, Journal: van de Vijver 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.09173 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-08-15 17:50:58 +02:00 (CEST) |
| Date last edited |
2022-09-27 17:44:49 +02:00 (CEST) |

Variant on transcripts
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