Variant #0000720054 (NC_000004.11:g.9892363_9892364dup, NC_000004.11(NM_001001290.1):c.1027-17_1027-16dup (SLC2A9))
| Chromosome |
4 |
| 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.9892363_9892364dup |
| DNA change (hg38) |
- |
| Published as |
SLC2A9(NM_020041.3):c.1114-17_1114-16dupCT |
| ISCN |
- |
| DB-ID |
SLC2A9_000015 |
| 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) |
Retrieve |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2021-02-08 18:36:18 +01:00 (CET) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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