RFX2 regulatory factor X2

Information
Symbol
RFX2
Type
protein-coding
Description
regulatory factor X2
Entrez Gene ID
5990
Genome
hg19
Position
chr19:5,993,175-6,110,511
Genome
hg38
Position
chr19:5,993,164-6,110,500
MIM
142765 OMIM
HGNC
HGNC:9983 HGNC
Ensembl
ENSG00000087903 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 12
Uncertain significance 0 94
Ranking
ClinVar
0
0
0
108
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
MIM 142765 OMIM
HGNC HGNC:9983 HGNC
Ensembl ENSG00000087903 Ensembl
AllianceGenome HGNC:9983
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000592546.5 hg38 chr19 5,994,502 6,110,532 116,031
ENST00000303657.10 hg38 chr19 5,993,164 6,110,500 117,337
ENST00000359161.7 hg38 chr19 5,993,517 6,049,232 55,716
ENST00000303657.10 hg19 chr19 5,993,175 6,110,511 117,337
ENST00000359161.7 hg19 chr19 5,993,528 6,049,243 55,716
ENST00000592546.5 hg19 chr19 5,994,513 6,110,543 116,031
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