MIR3937 microRNA 3937

Information
Symbol
MIR3937
Type
ncRNA
Description
microRNA 3937
Entrez Gene ID
100500822
Genome
hg19
Position
chrX:39,520,470-39,520,575
Genome
hg38
Position
chrX:39,661,216-39,661,321
HGNC
HGNC:38970 HGNC
Ensembl
ENSG00000263730 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 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:38970 HGNC
Ensembl ENSG00000263730 Ensembl
miRBase MI0016593
AllianceGenome HGNC:38970
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000580135.1 hg38 chrX 39,661,216 39,661,321 106
ENST00000580135.1 hg19 chrX 39,520,470 39,520,575 106
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