C17orf58 chromosome 17 open reading frame 58

Information
Symbol
C17orf58
Type
protein-coding
Description
chromosome 17 open reading frame 58
Entrez Gene ID
284018
Genome
hg19
Position
chr17:65,987,215-65,992,585
Genome
hg38
Position
chr17:67,991,099-67,996,469
HGNC
HGNC:27568 HGNC
Ensembl
ENSG00000186665 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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:27568 HGNC
Ensembl ENSG00000186665 Ensembl
AllianceGenome HGNC:27568
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000334461.7 hg38 chr17 67,991,130 67,993,649 2,520
ENST00000580729.3 hg38 chr17 67,991,099 67,996,469 5,371
ENST00000449250.3 hg38 chr17 67,991,336 67,993,545 2,210
ENST00000580729.3 hg19 chr17 65,987,215 65,992,585 5,371
ENST00000334461.7 hg19 chr17 65,987,246 65,989,765 2,520
ENST00000449250.3 hg19 chr17 65,987,452 65,989,661 2,210
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