GOLGA8T golgin A8 family member T

Information
Symbol
GOLGA8T
Type
protein-coding
Description
golgin A8 family member T
Entrez Gene ID
653075
Genome
hg19
Position
chr15:30,427,254-30,440,951
Genome
hg38
Position
chr15:30,135,051-30,148,748
HGNC
HGNC:44410 HGNC
Ensembl
ENSG00000261247 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 2 0
Ranking
ClinVar
0
0
0
6
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:44410 HGNC
Ensembl ENSG00000261247 Ensembl
AllianceGenome HGNC:44410
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000569052.2 hg38 chr15 30,135,051 30,148,748 13,698
ENST00000569052.2 hg19 chr15 30,427,254 30,440,951 13,698
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