Variant #0000655592 (NC_000006.11:g.42897382_42897384del, NM_000287.3:c.*34713_*34715del (PEX6))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42897382_42897384del
DNA change (hg38) g.42929644_42929646del
Published as CNPY3(NM_001318842.1):c.74_76delTGC (p.L25del), CNPY3(NM_006586.5):c.74_76del (p.(Leu25del))
ISCN -
DB-ID PTCRA_000002 See all 2 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX6 NM_000287.3 -?/. - c.*34713_*34715del r.(=) p.(=)
CNPY3 NM_006586.3 -?/. - c.74_76del r.(?) p.(Leu25del)
GNMT NM_018960.4 -?/. - c.-31124_-31122del r.(?) p.(=)
PTCRA NM_138296.2 -?/. - c.*3962_*3964del r.(=) p.(=)


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