Variant #0000995768 (NC_000006.11:g.42946751del, NM_000287.3:c.140del (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.42946751del
DNA change (hg38) -
Published as PEX6(NM_000287.3):c.140delC (p.(Pro47fs))
ISCN -
DB-ID GNMT_000024
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 2024-08-28 13:16:32 +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.140del r.(?) p.(Pro47Argfs*57)
PPP2R5D NM_006245.3 +?/. - c.-5665del r.(?) p.(=)
MEA1 NM_014623.2 +?/. - c.*33459del r.(?) p.(=)
GNMT NM_018960.4 +?/. - c.*15307del r.(?) p.(=)


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