Variant #0000091223 (NC_000005.9:g.142689725G>A, NM_001018077.1:c.1405C>T (NR3C1))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.142689725G>A
DNA change (hg38) g.143310160G>A
Published as -
ISCN -
DB-ID NR3C1_000004
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Jérôme Bouligand
Database submission license No license selected
Created by Jérôme Bouligand
Date created 2016-03-17 17:11:58 +01:00 (CET)
Date last edited 2016-03-29 21:00:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NR3C1 NM_001018077.1 +/. 4 c.1405C>T r.(?) p.(Arg469*)



Screenings

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