RNASEK-C17orf49 RNASEK-C17orf49 readthrough

Information
Symbol
RNASEK-C17orf49
Type
ncRNA
Description
RNASEK-C17orf49 readthrough
Entrez Gene ID
100529209
Genome
hg19
Position
chr17:6,917,052-6,920,839
Genome
hg38
Position
chr17:7,013,733-7,017,520
HGNC
HGNC:44419 HGNC
Ensembl
ENSG00000161939 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
SYNONYM BAP18
SYNONYM C17orf49
HGNC HGNC:44419 HGNC
Ensembl ENSG00000161939 Ensembl
AllianceGenome HGNC:44419
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000547302.3 hg38 chr17 7,013,733 7,017,520 3,788
ENST00000547302.3 hg19 chr17 6,917,052 6,920,839 3,788
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