GOLGA6D golgin A6 family member D

Information
Symbol
GOLGA6D
Type
protein-coding
Description
golgin A6 family member D
Entrez Gene ID
653643
Genome
hg19
Position
chr15:75,575,176-75,587,871
Genome
hg38
Position
chr15:75,282,835-75,295,530
HGNC
HGNC:32204 HGNC
Ensembl
ENSG00000140478 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 12
not provided 1 0
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
70
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:32204 HGNC
Ensembl ENSG00000140478 Ensembl
AllianceGenome HGNC:32204
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000434739.4 hg38 chr15 75,282,835 75,295,530 12,696
ENST00000434739.4 hg19 chr15 75,575,176 75,587,871 12,696
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