RFX8 regulatory factor X8

Information
Symbol
RFX8
Type
protein-coding
Description
regulatory factor X8
Entrez Gene ID
731220
Genome
hg19
Position
chr2:102,013,821-102,091,574
Genome
hg38
Position
chr2:101,397,359-101,475,112
HGNC
HGNC:37253 HGNC
Ensembl
ENSG00000196460 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 14
Uncertain significance 0 54
Ranking
ClinVar
0
0
2
68
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 :
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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:37253 HGNC
Ensembl ENSG00000196460 Ensembl
AllianceGenome HGNC:37253
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000428343.6 hg38 chr2 101,397,359 101,475,112 77,754
ENST00000646893.2 hg38 chr2 101,397,361 101,474,275 76,915
ENST00000646446.1 hg38 chr2 101,397,361 101,474,703 77,343
ENST00000428343.6 hg19 chr2 102,013,821 102,091,574 77,754
ENST00000646893.2 hg19 chr2 102,013,823 102,090,737 76,915
ENST00000646446.1 hg19 chr2 102,013,823 102,091,165 77,343
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