Variant #0000845823 (NC_000007.13:g.92134045C>A, NM_000466.2:c.-53C>G (PEX1))

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.92134045C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PEX1_000030 See all 20 reported entries
Variant remarks expression cloning luciferase assay 0.25 increased expression
Reference PubMed: Maxwell 2005
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 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 2022-04-06 20:03:53 +02:00 (CEST)
Date last edited 2022-04-07 15:54:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX1 NM_000466.2 +?/. 1 c.-53C>G r.=|[1.25] p.(=|inc)


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