Variant #0000885612 (NC_000003.11:g.155547508T>G, NM_004733.3:c.1451A>C (SLC33A1))
Chromosome |
3 |
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.155547508T>G |
DNA change (hg38) |
- |
Published as |
SLC33A1(NM_001190992.1):c.1451A>C (p.(Asn484Thr)), SLC33A1(NM_004733.3):c.1451A>C (p.N484T) |
ISCN |
- |
DB-ID |
SLC33A1_000004 See all 3 reported entries |
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) |
0.00175 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|