Variant #0001068033 (NC_000008.10:g.77896063del, NM_000318.2:c.352del (PEX2))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.77896063del
DNA change (hg38) -
Published as -
ISCN -
DB-ID PEX2_000054
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs755950154
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 12:55:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX2 NM_000318.2 +?/. - c.352del r.(?) p.(Glu118AsnfsTer12)


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