DHX58 DExH-box helicase 58

Information
Symbol
DHX58
Type
protein-coding
Description
DExH-box helicase 58
Entrez Gene ID
79132
Genome
hg19
Position
chr17:40,253,429-40,264,732
Genome
hg38
Position
chr17:42,101,411-42,112,714
MIM
608588 OMIM
HGNC
HGNC:29517 HGNC
Ensembl
ENSG00000108771 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 8
Uncertain significance 0 116
Ranking
ClinVar
0
0
0
126
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 :
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
SYNONYM D11LGP2
SYNONYM D11lgp2e
SYNONYM LGP2
SYNONYM RLR-3
MIM 608588 OMIM
HGNC HGNC:29517 HGNC
Ensembl ENSG00000108771 Ensembl
AllianceGenome HGNC:29517
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000251642.8 hg38 chr17 42,101,411 42,112,714 11,304
ENST00000251642.8 hg19 chr17 40,253,429 40,264,732 11,304
Genome browser