EAPP E2F associated phosphoprotein

Information
Symbol
EAPP
Type
protein-coding
Description
E2F associated phosphoprotein
Entrez Gene ID
55837
Genome
hg19
Position
chr14:34,985,144-35,008,907
Genome
hg38
Position
chr14:34,515,938-34,539,701
MIM
609486 OMIM
HGNC
HGNC:19312 HGNC
Ensembl
ENSG00000129518 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
30
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM BM036
SYNONYM C14orf11
MIM 609486 OMIM
HGNC HGNC:19312 HGNC
Ensembl ENSG00000129518 Ensembl
AllianceGenome HGNC:19312
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000250454.8 hg38 chr14 34,515,938 34,539,701 23,764
ENST00000250454.8 hg19 chr14 34,985,144 35,008,907 23,764
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