GOLGA8R golgin A8 family member R

Information
Symbol
GOLGA8R
Type
protein-coding
Description
golgin A8 family member R
Entrez Gene ID
101059918
Genome
hg19
Position
chr15:30,692,765-30,706,463
Genome
hg38
Position
chr15:30,400,562-30,414,260
HGNC
HGNC:44407 HGNC
Ensembl
ENSG00000186399 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 2 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:44407 HGNC
Ensembl ENSG00000186399 Ensembl
AllianceGenome HGNC:44407
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000327271.11 hg38 chr15 30,400,562 30,414,260 13,699
ENST00000327271.11 hg19 chr15 30,692,765 30,706,463 13,699
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