ATF7-NPFF ATF7-NPFF readthrough

Information
Symbol
ATF7-NPFF
Type
protein-coding
Description
ATF7-NPFF readthrough
Entrez Gene ID
114108587
Genome
hg19
Position
chr12:53,900,475-54,019,763
Genome
hg38
Position
chr12:53,506,691-53,625,979
HGNC
HGNC:55073 HGNC
Ensembl
ENSG00000267281 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 4
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
22
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 :
Filtering :
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
HGNC HGNC:55073 HGNC
Ensembl ENSG00000267281 Ensembl
AllianceGenome HGNC:55073
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000591834.1 hg38 chr12 53,506,691 53,625,979 119,289
ENST00000591834.1 hg19 chr12 53,900,475 54,019,763 119,289
Genome browser