Variant #0000238254 (NC_000010.10:g.94828318G>A, NM_183374.2:c.1433G>A (CYP26C1))

Chromosome 10
Allele Unknown
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.94828318G>A
DNA change (hg38) g.93068561G>A
Published as -
ISCN -
DB-ID CYP26C1_000002 See all 2 reported entries
Variant remarks expression cloning shows no CYP26C1 activity
Reference PubMed: Slavotinek 2013
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 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 2017-12-22 11:47:21 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP26C1 NM_183374.2 +/. 6 c.1433G>A r.(?) p.Arg478His -


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