Variant #0000163209 (NC_000001.10:g.43424429C>T, NM_006516.2:c.-107G>A (SLC2A1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43424429C>T |
| DNA change (hg38) |
g.42958758C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SLC2A1_000036 See all 3 reported entries |
| Variant remarks |
cDNA expression cloning in HEK293T cells shows preferential translation initiation at new ATG |
| Reference |
Kamsteeg submitted |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Erik-Jan Kamsteeg |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-02-20 09:39:11 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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