Variant #0000640619 (NC_000007.13:g.92151419del, PEX1(NM_000466.2):c.270del)

Individual ID 00283727
Chromosome 7
Allele Parent #1
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.92151419del
DNA change (hg38) g.92522105del
Published as 270delA
ISCN -
DB-ID PEX1_000060 See all 2 reported entries
Variant remarks -
Reference PubMed: Yik 2009, MORL Deafness Variation Database
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 +/. 2 c.270del r.(?) p.(Gln91Argfs*41)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000284877 DNA ? - - PEX1 2 Global Variome, with Curator vacancy