Variant #0000832487 (NC_000017.10:g.28564285_28564327del, NM_001045.6:- (SLC6A4))
Chromosome |
17 |
Allele |
Parent #1 |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
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 |
significantly reduced mRNA expression in lymphoblastoid cell lines |
Reference |
PubMed: Hu 2006 |
ClinVar ID |
- |
dbSNP ID |
- |
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 International |
Created by |
Johan den Dunnen |
Date created |
2022-01-07 09:35:10 +01:00 (CET) |
Date last edited |
2022-01-07 09:37:04 +01:00 (CET) |

Variant on transcripts
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