SNORD12B small nucleolar RNA, C/D box 12B

Information
Symbol
SNORD12B
Type
snoRNA
Description
small nucleolar RNA, C/D box 12B
Entrez Gene ID
100113393
Genome
hg19
Position
chr20:47,896,856-47,896,946
Genome
hg38
Position
chr20:49,280,319-49,280,409
HGNC
HGNC:33573 HGNC
Ensembl
ENSG00000222365 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
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
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:33573 HGNC
Ensembl ENSG00000222365 Ensembl
AllianceGenome HGNC:33573
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000410433.1 hg38 chr20 49,280,319 49,280,409 91
ENST00000410433.1 hg19 chr20 47,896,856 47,896,946 91
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