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
|