MIR3667HG MIR3667 host gene

Information
Symbol
MIR3667HG
Type
ncRNA
Description
MIR3667 host gene
Entrez Gene ID
348645
Genome
hg19
Position
chr22:50,013,290-50,018,568
Genome
hg38
Position
chr22:49,619,642-49,624,920
HGNC
HGNC:28010 HGNC
Ensembl
ENSG00000188511 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
SYNONYM C22orf34
HGNC HGNC:28010 HGNC
Ensembl ENSG00000188511 Ensembl
AllianceGenome HGNC:28010
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000405854.5 hg38 chr22 49,620,471 49,657,430 36,960
ENST00000343999.1 hg38 chr22 49,619,642 49,624,920 5,279
ENST00000414287.5 hg38 chr22 49,414,524 49,657,504 242,981
ENST00000414287.5 hg19 chr22 49,808,173 50,051,152 242,980
ENST00000343999.1 hg19 chr22 50,013,290 50,018,568 5,279
ENST00000405854.5 hg19 chr22 50,014,119 50,051,078 36,960
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