C17orf107 chromosome 17 open reading frame 107

Information
Symbol
C17orf107
Type
protein-coding
Description
chromosome 17 open reading frame 107
Entrez Gene ID
100130311
Genome
hg19
Position
chr17:4,802,831-4,806,229
Genome
hg38
Position
chr17:4,899,536-4,902,934
HGNC
HGNC:37238 HGNC
Ensembl
ENSG00000205710 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 176
Likely pathogenic 0 148
Benign 0 38
Likely benign 0 798
Conflicting classifications of pathogenicity 0 66
Uncertain significance 0 350
Ranking
ClinVar
0
0
196
1,250
14
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:37238 HGNC
Ensembl ENSG00000205710 Ensembl
AllianceGenome HGNC:37238
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000521575.1 hg38 chr17 4,899,418 4,900,799 1,382
ENST00000381365.4 hg38 chr17 4,899,536 4,902,934 3,399
ENST00000521575.1 hg19 chr17 4,802,713 4,804,094 1,382
ENST00000381365.4 hg19 chr17 4,802,831 4,806,229 3,399
KeyValue
strand+
start4,802,947
Gene SymbolC17orf107
Entrez GeneId100,130,311
Chr Band17p13.2
end4,806,226
chrchr17
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