Variant #0001035773 (NC_000006.11:g.42932527C>T, NC_000006.11(NM_000287.3):c.2806+1G>A (PEX6))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42932527C>T
DNA change (hg38) -
Published as PEX6(NM_000287.4):c.2806+1G>A
ISCN -
DB-ID CNPY3_000020 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX6 NM_000287.3 +?/. - c.2806+1G>A r.spl? p.?
CNPY3 NM_006586.3 +?/. - c.*25998C>T r.(=) p.(=)
GNMT NM_018960.4 +?/. - c.*1083C>T r.(=) p.(=)


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