Variant #0000150701 (NC_000007.13:g.75610876C>T, NM_000941.2:c.683C>T (POR))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.75610876C>T
DNA change (hg38) g.75981558C>T
Published as P228L
ISCN -
DB-ID POR_000040 See all 6 reported entries
Variant remarks cDNA expression cloning in bacteria showed cytochrome C reduction 0.75, NADPH oxidation 0.72
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) 0.00246 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 2024-10-10 01:58:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
POR NM_000941.2 -?/. 7 c.683C>T - r.(?) p.(Pro228Leu)


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