GOLGA8S golgin A8 family member S

Information
Symbol
GOLGA8S
Type
protein-coding
Description
golgin A8 family member S
Entrez Gene ID
653061
Genome
hg19
Position
chr15:23,599,895-23,613,488
Genome
hg38
Position
chr15:23,354,748-23,368,341
HGNC
HGNC:44409 HGNC
Ensembl
ENSG00000261739 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
not provided 1 0
Ranking
ClinVar
0
0
0
8
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:44409 HGNC
Ensembl ENSG00000261739 Ensembl
AllianceGenome HGNC:44409
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000562295.3 hg38 chr15 23,354,748 23,368,341 13,594
ENST00000562295.3 hg19 chr15 23,599,895 23,613,488 13,594
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