Variant #0000150732 (NC_000007.13:g.75615113G>A, NM_000941.2:c.1615G>A (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.75615113G>A
DNA change (hg38) g.75985795G>A
Published as G539R
ISCN -
DB-ID POR_000017 See all 5 reported entries
Variant remarks in vitro assay showed 17a-hydroxylase activity support 0.46, 17,20-lyase (P450c17) support 0.08
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 2024-03-06 21:29:09 +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 +/. 13 c.1615G>A - r.(?) p.(Gly539Arg)


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