RSPH10B2 radial spoke head 10 homolog B2

Information
Symbol
RSPH10B2
Type
protein-coding
Description
radial spoke head 10 homolog B2
Entrez Gene ID
728194
Genome
hg19
Position
chr7:6,793,740-6,838,394
Genome
hg38
Position
chr7:6,754,109-6,798,763
HGNC
HGNC:34385 HGNC
Ensembl
ENSG00000169402 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 12
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
74
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
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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
HGNC HGNC:34385 HGNC
Ensembl ENSG00000169402 Ensembl
AllianceGenome HGNC:34385
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000403107.5 hg38 chr7 6,754,109 6,798,763 44,655
ENST00000297186.7 hg38 chr7 6,757,590 6,798,765 41,176
ENST00000404077.6 hg38 chr7 6,754,103 6,798,765 44,663
ENST00000404077.6 hg19 chr7 6,793,734 6,838,396 44,663
ENST00000403107.5 hg19 chr7 6,793,740 6,838,394 44,655
ENST00000297186.7 hg19 chr7 6,797,221 6,838,396 41,176
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