Variant #0000854788 (NC_000017.10:g.26732944C>G, NM_080669.4:c.189G>C (SLC46A1))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.26732944C>G |
DNA change (hg38) |
- |
Published as |
SLC46A1(NM_080669.3):c.189G>C (p.R63S) |
ISCN |
- |
DB-ID |
SLC46A1_000022 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00172 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-05-09 15:47:41 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|