C17orf99 chromosome 17 open reading frame 99

Information
Symbol
C17orf99
Type
protein-coding
Description
chromosome 17 open reading frame 99
Entrez Gene ID
100141515
Genome
hg19
Position
chr17:76,142,466-76,162,378
Genome
hg38
Position
chr17:78,146,385-78,166,297
HGNC
HGNC:34490 HGNC
Ensembl
ENSG00000187997 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
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
[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
SYNONYM IL-40
SYNONYM UNQ464
HGNC HGNC:34490 HGNC
Ensembl ENSG00000187997 Ensembl
AllianceGenome HGNC:34490
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000340363.10 hg38 chr17 78,146,385 78,166,297 19,913
ENST00000340363.10 hg19 chr17 76,142,466 76,162,378 19,913
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