Variant #0001068031 (NC_000007.13:g.92123799A>G, NC_000007.13(NM_000466.2):c.2926+2T>C (PEX1))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.92123799A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID PEX1_000014 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs267608180
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-02 12:46:02 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX1 NM_000466.2 +/. - c.2926+2T>C r.(?) p.(?)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.