Variant #0000150700 (NC_000007.13:g.75610390T>G, NM_000941.2:c.541T>G (POR))

Chromosome 7
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.75610390T>G
DNA change (hg38) g.75981072T>G
Published as Y181D
ISCN -
DB-ID POR_000062 See all 4 reported entries
Variant remarks cDNA expression cloning in bacteria showed defective cytochrome C reduction/NADPH oxidation
Reference PubMed: Huang 2005
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-12-17 13:43:34 +01:00 (CET)
Date last edited 2022-10-13 02:55:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
POR NM_000941.2 +/. 6 c.541T>G - r.(?) p.(Tyr181Asp)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.