HROB homologous recombination factor with OB-fold

Information
Symbol
HROB
Type
protein-coding
Description
homologous recombination factor with OB-fold
Entrez Gene ID
78995
Genome
hg19
Position
chr17:42,219,274-42,239,844
Genome
hg38
Position
chr17:44,141,906-44,162,476
MIM
618611 OMIM
HGNC
HGNC:28460 HGNC
Ensembl
ENSG00000125319 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
6
2
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 C17orf53
SYNONYM MCM8IP
MIM 618611 OMIM
HGNC HGNC:28460 HGNC
Ensembl ENSG00000125319 Ensembl
AllianceGenome HGNC:28460
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585683.6 hg38 chr17 44,141,930 44,162,476 20,547
ENST00000245382.6 hg38 chr17 44,142,022 44,162,476 20,455
ENST00000319977.8 hg38 chr17 44,141,906 44,162,476 20,571
ENST00000319977.8 hg19 chr17 42,219,274 42,239,844 20,571
ENST00000585683.6 hg19 chr17 42,219,298 42,239,844 20,547
ENST00000245382.6 hg19 chr17 42,219,390 42,239,844 20,455
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