ZNF677 zinc finger protein 677

Information
Symbol
ZNF677
Type
protein-coding
Description
zinc finger protein 677
Entrez Gene ID
342926
Genome
hg19
Position
chr19:53,738,634-53,758,126
Genome
hg38
Position
chr19:53,235,381-53,254,873
HGNC
HGNC:28730 HGNC
Ensembl
ENSG00000197928 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 14
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
74
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
HGNC HGNC:28730 HGNC
Ensembl ENSG00000197928 Ensembl
AllianceGenome HGNC:28730
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000598806.5 hg38 chr19 53,242,081 53,254,879 12,799
ENST00000594681.5 hg38 chr19 53,241,924 53,254,831 12,908
ENST00000601413.5 hg38 chr19 53,243,556 53,254,821 11,266
ENST00000601828.5 hg38 chr19 53,243,333 53,254,846 11,514
ENST00000599012.5 hg38 chr19 53,241,392 53,254,860 13,469
ENST00000333952.8 hg38 chr19 53,235,385 53,251,630 16,246
ENST00000598513.6 hg38 chr19 53,235,381 53,254,873 19,493
ENST00000598513.6 hg19 chr19 53,738,634 53,758,126 19,493
ENST00000333952.8 hg19 chr19 53,738,638 53,754,883 16,246
ENST00000599012.5 hg19 chr19 53,744,645 53,758,113 13,469
ENST00000594681.5 hg19 chr19 53,745,177 53,758,084 12,908
ENST00000598806.5 hg19 chr19 53,745,334 53,758,132 12,799
ENST00000601828.5 hg19 chr19 53,746,586 53,758,099 11,514
ENST00000601413.5 hg19 chr19 53,746,809 53,758,074 11,266
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