Variant #0000299523 (NC_000020.10:g.45354829C>G, NM_030777.3:c.1154C>G (SLC2A10))
Chromosome |
20 |
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.45354829C>G |
DNA change (hg38) |
g.46726190C>G |
Published as |
SLC2A10(NM_030777.3):c.1154C>G (p.(Ala385Gly)), SLC2A10(NM_030777.4):c.1154C>G (p.A385G) |
ISCN |
- |
DB-ID |
SLC2A10_000025 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) |
0.01139 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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