Variant #0000686488 (NC_000001.10:g.2338289dup, PEX10(NM_153818.1):c.706dup)

Individual ID 00310035
Chromosome 1
Allele Both (homozygous)
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.2338289dup
DNA change (hg38) -
Published as 646_647insA
ISCN -
DB-ID PEX10_000036
Variant remarks no variant 2nd chromosome reported
Reference PubMed: Ebberink 2011
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     
PEX10 NM_153818.1 +/. - c.706dup r.(?) p.(Ser236Lysfs*123)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000311183 DNA SEQ - - PEX10 1 Johan den Dunnen