Variant #0000832438 (NC_000017.10:g.28564285_28564327del, NM_001045.6:- (SLC6A4))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.28564285_28564327del
DNA change (hg38) g.30237267_30237309del
Published as short 1917_-1875del
ISCN -
DB-ID SLC6A4_000004 See all 5 reported entries
Variant remarks expression analysis in human placental chorio-carcinoma cell line (JAR) showed reduced expression to 0.33
Reference PubMed: Heils 1996
ClinVar ID -
dbSNP ID rs774676466
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-01-06 18:04:01 +01:00 (CET)
Date last edited 2022-01-07 09:18:37 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC6A4 NM_001045.6 +/. _1 - r.? p.?


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