Full data view for gene PEX2

This database is one of the dbPEX gene variant databases.
Information The variants shown are described using the NM_000318.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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     
+/. 4 c.286C>T r.(?) p.(Gln96*) Both (homozygous) - pathogenic (recessive) g.77896129G>A - - - PEX2_000016 - PubMed: Ebberink 2011 - - Germline - - - 0 - DNA SEQ - - PBD - PubMed: Ebberink 2011 - - - - - - 0 - - 1 Shandi Hiebler
+/. - c.286C>T r.(?) p.(Gln96Ter) Unknown - pathogenic g.77896129G>A - PEX2(NM_000318.2):c.286C>T (p.(Gln96Ter)), PEX2(NM_001172086.1):c.286C>T (p.Q96*) - PEX2_000016 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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