RPL17-C18orf32 RPL17-C18orf32 readthrough

Information
Symbol
RPL17-C18orf32
Type
protein-coding
Description
RPL17-C18orf32 readthrough
Entrez Gene ID
100526842
Genome
hg19
Position
chr18:47,008,051-47,017,956
Genome
hg38
Position
chr18:49,481,681-49,491,586
HGNC
HGNC:44661 HGNC
Ensembl
ENSG00000215472 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Uncertain significance 0 12
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
SYNONYM PD-1
SYNONYM RPL17
HGNC HGNC:44661 HGNC
Ensembl ENSG00000215472 Ensembl
AllianceGenome HGNC:44661
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584895.5 hg38 chr18 49,481,681 49,491,586 9,906
ENST00000332968.11 hg38 chr18 49,482,152 49,492,479 10,328
ENST00000584895.5 hg19 chr18 47,008,051 47,017,956 9,906
ENST00000332968.11 hg19 chr18 47,008,522 47,018,849 10,328
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