GOLGA8M golgin A8 family member M

Information
Symbol
GOLGA8M
Type
protein-coding
Description
golgin A8 family member M
Entrez Gene ID
653720
Genome
hg19
Position
chr15:28,943,729-28,957,567
Genome
hg38
Position
chr15:28,698,583-28,712,421
HGNC
HGNC:44404 HGNC
Ensembl
ENSG00000188626 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 14
not provided 3 0
Ranking
ClinVar
0
0
0
14
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:44404 HGNC
Ensembl ENSG00000188626 Ensembl
AllianceGenome HGNC:44404
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000563027.2 hg38 chr15 28,698,583 28,712,421 13,839
ENST00000563027.2 hg19 chr15 28,943,729 28,957,567 13,839
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