Variant #0000640615 (NC_000007.13:g.92148336G>C, PEX1(NM_000466.2):c.330C>G)

Individual ID 00283723
Chromosome 7
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.92148336G>C
DNA change (hg38) g.92519022G>C
Published as -
ISCN -
DB-ID PEX1_000118 See all 3 reported entries
Variant remarks -
Reference MORL Deafness Variation Database, PubMed: Bean 2013
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00224 View details
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 -/- 3 c.330C>G r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000284873 DNA ? - - PEX1 1 Global Variome, with Curator vacancy