Variant #0000687369 (NC_000001.10:g.2338015T>C, PEX10(NM_153818.1):c.880A>G)

Individual ID 00310666
Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2338015T>C
DNA change (hg38) g.2406576T>C
Published as -
ISCN -
DB-ID PEX10_000014 See all 5 reported entries
Variant remarks 820A>G
Reference PubMed: Yik 2009
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 0.03
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02024 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX10 NM_153818.1 -/. - c.880A>G r.(?) p.(Thr294Ala)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000311818 DNA SEQ - - PEX10 1 Johan den Dunnen