Variant #0000164213 (NC_000007.13:g.92132486dup, NM_000466.2:c.2097dup (PEX1))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.92132486dup
DNA change (hg38) g.92503172dup
Published as -
ISCN -
DB-ID PEX1_000002 See all 165 reported entries
Variant remarks cDNA expression cloning in PEX1 defective fibroblatst showed no complementation (0.00)
Reference PubMed: Ratbi 2015, Journal: Ratbi 2015
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-03-19 16:50:04 +01:00 (CET)
Date last edited 2020-09-10 15:04:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX1 NM_000466.2 +/. 13 c.2097dup r.(?) p.Ile700Tyrfs*42


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