Variant #0000977249 (NC_000006.11:g.42937459del, NM_000287.3:c.1315del (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.42937459del
DNA change (hg38) -
Published as PEX6(NM_000287.4):c.1315del (p.(Glu439Argfs*11))
ISCN -
DB-ID GNMT_000020
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 2024-04-19 20:27:30 +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.1315del r.(?) p.(Glu439Argfs*11)
GNMT NM_018960.4 +?/. - c.*6015del r.(?) p.(=)


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