LOC730098 uncharacterized LOC730098

Information
Symbol
LOC730098
Type
protein-coding
Description
uncharacterized LOC730098
Entrez Gene ID
730098
Genome
hg19
Position
chr9:34,664,160-34,666,042
Genome
hg38
Position
chr9:34,664,163-34,666,045
Ensembl
ENSG00000187186 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
Ensembl ENSG00000187186 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000423809.5 hg38 chr9 34,665,028 34,666,112 1,085
ENST00000421828.7 hg38 chr9 34,664,163 34,666,045 1,883
ENST00000544078.2 hg38 chr9 34,665,032 34,666,028 997
ENST00000416454.5 hg38 chr9 34,665,028 34,666,028 1,001
ENST00000421828.7 hg19 chr9 34,664,160 34,666,042 1,883
ENST00000416454.5 hg19 chr9 34,665,025 34,666,025 1,001
ENST00000423809.5 hg19 chr9 34,665,025 34,666,109 1,085
ENST00000544078.2 hg19 chr9 34,665,029 34,666,025 997
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