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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC6A8 NM_005629.3 +/+ 2 c.321_323del r.(?) p.Phe107del


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