Variant #0000413191 (NC_000001.10:g.60377389A>T, NM_000775.2:c.575T>A (CYP2J2))

Chromosome 1
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.60377389A>T
DNA change (hg38) g.59911717A>T
Published as 15030T>A (I192N)
ISCN -
DB-ID CYP2J2_000005 See all 2 reported entries
Variant remarks Enzime activity in_vitro: Reduced AA metabolism 
Reference PubMed: King 2002
ClinVar ID -
dbSNP ID rs66515830
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Julia Lopez
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2018-11-01 17:40:32 +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     
CYP2J2 NM_000775.2 -?/-? 4 c.575T>A r.(=) p.(Ile192Asn) CYP2J2*4


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