C17orf50 chromosome 17 open reading frame 50

Information
Symbol
C17orf50
Type
protein-coding
Description
chromosome 17 open reading frame 50
Entrez Gene ID
146853
Genome
hg19
Position
chr17:34,087,906-34,092,098
Genome
hg38
Position
chr17:35,760,887-35,765,079
HGNC
HGNC:29581 HGNC
Ensembl
ENSG00000270806 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
14
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:29581 HGNC
Ensembl ENSG00000270806 Ensembl
AllianceGenome HGNC:29581
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000603305.1 hg38 chr17 35,760,909 35,764,597 3,689
ENST00000604830.1 hg38 chr17 35,760,897 35,764,614 3,718
ENST00000605587.2 hg38 chr17 35,760,887 35,765,079 4,193
ENST00000605587.2 hg19 chr17 34,087,906 34,092,098 4,193
ENST00000604830.1 hg19 chr17 34,087,916 34,091,633 3,718
ENST00000603305.1 hg19 chr17 34,087,928 34,091,616 3,689
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