Variant #0000436032 (NC_000003.11:g.49570882T>C, NM_004393.5:c.*250T>C (DAG1))

Chromosome 3
Allele Unknown
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.49570882T>C
DNA change (hg38) g.49533449T>C
Published as 3332C>T
ISCN -
DB-ID DAG1_000006 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1050088
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.53873 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-11-03 16:20:45 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAG1 NM_004393.5 ?/. 6 c.*250T>C r.(?) p.(=)


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