Variant #0000413185 (NC_000023.10:g.152955888_152955890del, NM_005629.3:c.321_323del (SLC6A8))
| Chromosome |
X |
| Allele |
Maternal (confirmed) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.152955888_152955890del |
| DNA change (hg38) |
g.153690433_153690435del |
| Published as |
319_321delCTT |
| ISCN |
- |
| DB-ID |
SLC6A8_003018 See all 14 reported entries |
| Variant remarks |
overexpression in SLC6A8 deficient fibroblasts did not restore creatine uptake |
| Reference |
PubMed: Rosenberg 2007 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Gajja Salomons |
| Database submission license |
No license selected |
| Created by |
Gajja Salomons |
| Date created |
2016-01-26 15:07:51 +01:00 (CET) |
| Date last edited |
2020-07-21 13:25:21 +02:00 (CEST) |

Variant on transcripts
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