C17orf78 chromosome 17 open reading frame 78

Information
Symbol
C17orf78
Type
protein-coding
Description
chromosome 17 open reading frame 78
Entrez Gene ID
284099
Genome
hg19
Position
chr17:35,732,927-35,749,662
Genome
hg38
Position
chr17:37,375,985-37,392,708
HGNC
HGNC:26831 HGNC
Ensembl
ENSG00000278505 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
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 :
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:26831 HGNC
Ensembl ENSG00000278505 Ensembl
AllianceGenome HGNC:26831
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000615133.2 hg38 chr17 37,375,985 37,392,708 16,724
ENST00000611038.4 hg38 chr17 37,375,986 37,392,706 16,721
ENST00000615133.2 hg19 chr17 35,732,927 35,749,662 16,736
ENST00000611038.4 hg19 chr17 35,732,928 35,749,660 16,733
Genome browser