HELB DNA helicase B

Information
Symbol
HELB
Type
protein-coding
Description
DNA helicase B
Entrez Gene ID
92797
Genome
hg19
Position
chr12:66,696,273-66,731,979
Genome
hg38
Position
chr12:66,302,493-66,338,199
MIM
614539 OMIM
HGNC
HGNC:17196 HGNC
Ensembl
ENSG00000127311 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 6
Uncertain significance 0 120
Ranking
ClinVar
0
0
0
136
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 DHB
SYNONYM hDHB
MIM 614539 OMIM
HGNC HGNC:17196 HGNC
Ensembl ENSG00000127311 Ensembl
AllianceGenome HGNC:17196
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000247815.9 hg38 chr12 66,302,493 66,338,199 35,707
ENST00000247815.9 hg19 chr12 66,696,273 66,731,979 35,707
Genome browser