AATF apoptosis antagonizing transcription factor

Information
Symbol
AATF
Type
protein-coding
Description
apoptosis antagonizing transcription factor
Entrez Gene ID
26574
Genome
hg19
Position
chr17:35,306,254-35,414,171
Genome
hg38
Position
chr17:36,948,954-37,056,871
MIM
608463 OMIM
HGNC
HGNC:19235 HGNC
Ensembl
ENSG00000275700 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 88
Ranking
ClinVar
0
0
0
88
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
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 BFR2
SYNONYM CHE-1
SYNONYM CHE1
SYNONYM DED
MIM 608463 OMIM
HGNC HGNC:19235 HGNC
Ensembl ENSG00000275700 Ensembl
AllianceGenome HGNC:19235
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000681062.1 hg38 chr17 36,949,285 37,056,860 107,576
ENST00000616434.2 hg38 chr17 36,948,925 37,056,858 107,934
ENST00000679997.1 hg38 chr17 36,949,008 37,056,871 107,864
ENST00000680340.1 hg38 chr17 36,948,925 37,056,870 107,946
ENST00000679881.1 hg38 chr17 36,949,290 37,056,860 107,571
ENST00000680782.1 hg38 chr17 36,949,301 37,056,860 107,560
ENST00000619387.5 hg38 chr17 36,948,954 37,056,871 107,918
ENST00000619387.5 hg19 chr17 35,306,254 35,414,171 107,918
ENST00000679881.1 hg19 chr17 35,306,590 35,414,160 107,571
ENST00000679997.1 hg19 chr17 35,306,308 35,414,171 107,864
ENST00000680340.1 hg19 chr17 35,306,225 35,414,170 107,946
ENST00000616434.2 hg19 chr17 35,306,225 35,414,158 107,934
ENST00000681062.1 hg19 chr17 35,306,585 35,414,160 107,576
ENST00000680782.1 hg19 chr17 35,306,601 35,414,160 107,560
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