All variants in the PAGE1 gene

Information The variants shown are described using the NM_003785.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

Owner     
-?/. - c.413A>G r.(?) p.(Glu138Gly) - likely benign g.49454026T>C g.49689423T>C PAGE1(NM_003785.3):c.413A>G (p.(Glu138Gly)) - PAGE1_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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