Variant #0000686417 (NC_000008.10:g.77896252C>T, PEX2(NM_000318.2):c.163G>A)

Individual ID 00309960
Chromosome 8
Allele Parent #2
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.77896252C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID PEX2_000004
Variant remarks -
Reference PubMed: Imamura 1998
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX2 NM_000318.2 +/. - c.163G>A r.163g>a p.Glu55Lys



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000311108 DNA;RNA RT-PCR;SEQ - - PEX2 2 Nancy Braverman