DDX27 DEAD-box helicase 27

Information
Symbol
DDX27
Type
protein-coding
Description
DEAD-box helicase 27
Entrez Gene ID
55661
Genome
hg19
Position
chr20:47,835,953-47,860,610
Genome
hg38
Position
chr20:49,219,416-49,244,073
MIM
616621 OMIM
HGNC
HGNC:15837 HGNC
Ensembl
ENSG00000124228 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 4
not provided 1 0
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
72
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
SYNONYM DRS1
SYNONYM Drs1p
SYNONYM HSPC259
SYNONYM PP3241
SYNONYM RHLP
SYNONYM dJ686N3.1
MIM 616621 OMIM
HGNC HGNC:15837 HGNC
Ensembl ENSG00000124228 Ensembl
AllianceGenome HGNC:15837
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000618172.5 hg38 chr20 49,219,416 49,244,073 24,658
ENST00000618172.5 hg19 chr20 47,835,953 47,860,610 24,658
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