Variant #0000150702 (NC_000007.13:g.75611597A>G, NM_000941.2:c.787A>G (POR))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.75611597A>G
DNA change (hg38) g.75982279A>G
Published as M263V
ISCN -
DB-ID POR_000042 See all 4 reported entries
Variant remarks cDNA expression cloning in bacteria showed cytochrome C reduction 0.76, NADPH oxidation 0.57
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) 2.0E-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 2016-12-17 13:43:34 +01:00 (CET)
Date last edited 2024-02-14 11:33:15 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
POR NM_000941.2 +?/. 8 c.787A>G - r.(?) p.(Met263Val)


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