Variant #0000624484 (NC_000023.10:g.152959440_152959442del, NM_005629.3:c.1222_1224del (SLC6A8))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.152959440_152959442del
DNA change (hg38) g.153693985_153693987del
Published as SLC6A8(NM_005629.4):c.1222_1224delTTC (p.F408del)
ISCN -
DB-ID SLC6A8_003082 See all 17 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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 +/. - c.1222_1224del r.(?) p.(Phe408del)


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