Variant #0000331683 (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 pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.92132486dup
DNA change (hg38) g.92503172dup
Published as PEX1(NM_000466.3):c.2097dup (p.(Ile700TyrfsTer42)), PEX1(NM_000466.3):c.2097dupT (p.I700Yfs*42), PEX1(NM_001282678.1):c.1473dupT (p.I492Yfs*42), PE...
ISCN -
DB-ID PEX1_000002 See all 163 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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 +/. - c.2097dup r.(?) p.(Ile700TyrfsTer42)


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