Variant #0000413194 (NC_000001.10:g.60392494C>A, NM_000775.2:c.-76G>T (CYP2J2))

Chromosome 1
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.60392494C>A
DNA change (hg38) g.59926822C>A
Published as -76G>T
ISCN -
DB-ID CYP2J2_000009 See all 2 reported entries
Variant remarks Enzime activity in_vitro: Reduced transcription due to loss of Sp1 binding site
Reference PubMed: King 2002, PubMed: Spiecker 2004
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 +/+ 1 c.-76G>T r.(=) p.(=) CYP2J2*7


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