ZNF772 zinc finger protein 772

Information
Symbol
ZNF772
Type
protein-coding
Description
zinc finger protein 772
Entrez Gene ID
400720
Genome
hg19
Position
chr19:57,980,954-57,988,938
Genome
hg38
Position
chr19:57,469,586-57,477,570
HGNC
HGNC:33106 HGNC
Ensembl
ENSG00000197128 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
50
2
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:33106 HGNC
Ensembl ENSG00000197128 Ensembl
AllianceGenome HGNC:33106
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000425074.3 hg38 chr19 57,473,150 57,477,566 4,417
ENST00000600175.5 hg38 chr19 57,466,663 57,477,551 10,889
ENST00000610548.2 hg38 chr19 57,473,274 57,477,570 4,297
ENST00000601768.1 hg38 chr19 57,466,832 57,477,504 10,673
ENST00000356584.8 hg38 chr19 57,469,586 57,477,566 7,981
ENST00000427512.6 hg38 chr19 57,469,586 57,477,570 7,985
ENST00000343280.8 hg38 chr19 57,469,586 57,477,570 7,985
ENST00000600175.5 hg19 chr19 57,978,031 57,988,919 10,889
ENST00000601768.1 hg19 chr19 57,978,200 57,988,872 10,673
ENST00000356584.8 hg19 chr19 57,980,954 57,988,934 7,981
ENST00000343280.8 hg19 chr19 57,980,954 57,988,938 7,985
ENST00000427512.6 hg19 chr19 57,980,954 57,988,938 7,985
ENST00000425074.3 hg19 chr19 57,984,518 57,988,934 4,417
ENST00000610548.2 hg19 chr19 57,984,642 57,988,938 4,297
Genome browser