Variant #0000436038 (NC_000003.11:g.49568519C>T, NM_001165928.3:c.575C>T (DAG1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.49568519C>T
DNA change (hg38) g.49531086C>T
Published as -
ISCN -
DB-ID DAG1_000011 See all 3 reported entries
Variant remarks expression cloning (DAG1 negative cells) shows normal protein localisation/stability
Reference PubMed: Hara 2011
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 2011-03-25 18:07:54 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAG1 NM_001165928.3 -/. 6 c.575C>T r.(575c>u) p.Thr192Met


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