Variant #0000988457 (NC_000009.11:g.133319980_133320457del, NM_000050.4:c.-356_-68+75{0} (ASS1))

Chromosome 9
Allele Both (homozygous)
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.133319980_133320457del
DNA change (hg38) g.130444593_130445070del
Published as hg19 133319979-133320456del
ISCN -
DB-ID ASS1_000205 See all 3 reported entries
Variant remarks expression cloning (A2058 and HepG2 cells) shows reduced reporter expression (0.033-0.036)
Reference PubMed: Imagawa 2020
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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-07-09 17:10:41 +02:00 (CEST)
Date last edited 2024-07-09 17:19:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASS1 NM_000050.4 +/. _1_1i c.-356_-68+75{0} - p.=|0.03


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