Variant #0000193790 (NC_000011.9:g.14907393A>G, NM_024514.4:c.296T>C (CYP2R1))

Chromosome 11
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.14907393A>G
DNA change (hg38) g.14885847A>G
Published as -
ISCN -
DB-ID CYP2R1_000002 See all 6 reported entries
Variant remarks expression cloning HEK293 cells no activity
Reference PubMed: Cheng 2004
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00026 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 2017-08-25 12:39:56 +02:00 (CEST)
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     
CYP2R1 NM_024514.4 +/. 2 c.296T>C r.(?) p.Leu99Pro -


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