Variant #0001064548 (NC_000006.11:g.42897382_42897384dup, NM_000287.3:c.*34713_*34715dup (PEX6))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.42897382_42897384dup
DNA change (hg38) -
Published as CNPY3(NM_006586.5):c.74_76dup (p.(Leu25dup))
ISCN -
DB-ID PTCRA_000003
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX6 NM_000287.3 ?/. - c.*34713_*34715dup r.(=) p.(=)
CNPY3 NM_006586.3 ?/. - c.74_76dup r.(?) p.(Leu25dup)
GNMT NM_018960.4 ?/. - c.-31124_-31122dup r.(?) p.(=)
PTCRA NM_138296.2 ?/. - c.*3962_*3964dup r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.