Variant #0000640598 (NC_000007.13:g.92146919_92146920del, PEX1(NM_000466.2):c.911_912del)

Individual ID 00283706
Chromosome 7
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.92146919_92146920del
DNA change (hg38) g.92517605_92517606del
Published as -
ISCN -
DB-ID PEX1_000274
Variant remarks -
Reference MORL Deafness Variation Database, PubMed: Rosewich 2005, PubMed: Steinberg 1993, 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 Global Variome, with Curator vacancy
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX1 NM_000466.2 +/+ 5 c.911_912del r.(?) p.(Ser304Cysfs*4)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000284856 DNA ? - - PEX1 1 Global Variome, with Curator vacancy