E2F7 E2F transcription factor 7

Information
Symbol
E2F7
Type
protein-coding
Description
E2F transcription factor 7
Entrez Gene ID
144455
Genome
hg19
Position
chr12:77,415,031-77,459,349
Genome
hg38
Position
chr12:77,021,251-77,065,569
MIM
612046 OMIM
HGNC
HGNC:23820 HGNC
Ensembl
ENSG00000165891 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 6
Uncertain significance 0 90
Ranking
ClinVar
0
0
0
108
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
MIM 612046 OMIM
HGNC HGNC:23820 HGNC
Ensembl ENSG00000165891 Ensembl
AllianceGenome HGNC:23820
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000416496.6 hg38 chr12 77,021,248 77,065,563 44,316
ENST00000322886.12 hg38 chr12 77,021,251 77,065,569 44,319
ENST00000416496.6 hg19 chr12 77,415,028 77,459,343 44,316
ENST00000322886.12 hg19 chr12 77,415,031 77,459,349 44,319
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