Variant #0000436033 (NC_000003.11:g.49571462G>T, NM_004393.5:c.*830G>T (DAG1))

Chromosome 3
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.49571462G>T
DNA change (hg38) g.49534029G>T
Published as -
ISCN -
DB-ID DAG1_000007
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs12583
Origin Germline
Segregation -
Frequency 0.30-0.42
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 2009-09-04 15:04:34 +02:00 (CEST)
Date last edited 2012-11-02 20:40:47 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAG1 NM_004393.5 ?/. 6 c.*830G>T r.(?) p.(=)


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