Variant #0000879690 (NC_000011.9:g.45832838G>A, NM_018389.4:c.1047G>A (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.45832838G>A |
| DNA change (hg38) |
g.45811287G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SLC35C1_000023 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Roos 2023, Journal: Roos 2023 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00091 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-09-27 17:43:45 +02:00 (CEST) |
| Date last edited |
2025-01-23 20:41:23 +01:00 (CET) |

Variant on transcripts
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