HDDC3 HD domain containing 3

Information
Symbol
HDDC3
Type
protein-coding
Description
HD domain containing 3
Entrez Gene ID
374659
Genome
hg19
Position
chr15:91,473,198-91,475,779
Genome
hg38
Position
chr15:90,929,968-90,932,549
HGNC
HGNC:30522 HGNC
Ensembl
ENSG00000184508 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 6
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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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
SYNONYM (ppGpp)ase
SYNONYM MESH1
SYNONYM MYNRL15
HGNC HGNC:30522 HGNC
Ensembl ENSG00000184508 Ensembl
AllianceGenome HGNC:30522
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000559898.5 hg38 chr15 90,931,099 90,932,550 1,452
ENST00000394272.8 hg38 chr15 90,929,968 90,932,549 2,582
ENST00000330334.7 hg38 chr15 90,930,925 90,932,546 1,622
ENST00000646620.1 hg38 chr15 90,930,918 90,935,130 4,213
ENST00000394272.8 hg19 chr15 91,473,198 91,475,779 2,582
ENST00000646620.1 hg19 chr15 91,474,148 91,478,360 4,213
ENST00000330334.7 hg19 chr15 91,474,155 91,475,776 1,622
ENST00000559898.5 hg19 chr15 91,474,329 91,475,780 1,452
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