Variant #0000640271 (NC_000006.11:g.42946578del, PEX6(NM_000287.3):c.311del)

Individual ID 00283379
Chromosome 6
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42946578del
DNA change (hg38) -
Published as 311delG
ISCN -
DB-ID PEX6_000224
Variant remarks no variant 2nd chromosome reported
Reference MORL Deafness Variation Database, PubMed: Ebberink 2010
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Global Variome, with Curator vacancy
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX6 NM_000287.3 +/. 1 c.311del r.(?) p.(Gly104Valfs*22)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000284529 DNA SEQ - - PEX6 1 Global Variome, with Curator vacancy