Full data view for gene PEX19

This database is one of the dbPEX gene variant databases.
Information The variants shown are described using the NM_002857.3 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. - c.254C>T r.(?) p.(Ala85Val) Both (homozygous) ACMG VUS g.160252826G>A - - - PEX19_000006 ACMG PM2, PP3, PP4, BP1; The sib-pair's electroclinical phenotype is different to the previously reported phenotype in a single case, with childhood onset, no dysmorphic features and a less rapidly progressive clinical course. However, the same predicted damaging missense variant is homozygous in four unrelated families (two reported here) with similar presentation from Malta; the same haplotype was confirmed supporting a founder effect. The variant was not present in the Maltese human genome project (n=400). It is therefore with high confidence we expand the PEX19 clinical spectrum to PME. PubMed: Courage 2021, Journal: Courage 2021 - - Germline - - - - - DNA SEQ, SEQ-NG WES sibling pair - PBD12A PME21 PubMed: Courage 2021, Journal: Courage 2021 family, 2 affected (2M) M yes Malta - - - - - 2 Carolina Courage
?/. - c.254C>T r.(?) p.(Ala85Val) Both (homozygous) ACMG VUS g.160252826G>A - - - PEX19_000006 ACMG PM2, PP3, PP4, BP1; The sib-pair's electroclinical phenotype is different to the previously reported phenotype in a single case, with childhood onset, no dysmorphic features and a less rapidly progressive clinical course. However, the same predicted damaging missense variant is homozygous in four unrelated families (two reported here) with similar presentation from Malta; the same haplotype was confirmed supporting a founder effect. The variant was not present in the Maltese human genome project (n=400). It is therefore with high confidence we expand the PEX19 clinical spectrum to PME. PubMed: Courage 2021, Journal: Courage 2021 - - Germline - - - - - DNA SEQ, SEQ-NG WES sibling pair - PBD12A PME22 PubMed: Courage 2021, Journal: Courage 2021 relative of PME21 M yes Malta - - - - - 1 Carolina Courage
?/. - c.254C>T r.(?) p.(Ala85Val) Both (homozygous) ACMG VUS g.160252826G>A - - - PEX19_000006 ACMG PM2, PP3, PP4, BP1; The sib-pair's electroclinical phenotype is different to the previously reported phenotype in a single case, with childhood onset, no dysmorphic features and a less rapidly progressive clinical course. However, the same predicted damaging missense variant is homozygous in four unrelated families (two reported here) with similar presentation from Malta; the same haplotype was confirmed supporting a founder effect. The variant was not present in the Maltese human genome project (n=400). It is therefore with high confidence we expand the PEX19 clinical spectrum to PME. PubMed: Courage 2021, Journal: Courage 2021 - - Germline - - - - - DNA SEQ, SEQ-NG WES - PBD12A PME60 PubMed: Courage 2021, Journal: Courage 2021 - F no Malta - - - - - 1 Carolina Courage
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