RFESD Rieske Fe-S domain containing

Information
Symbol
RFESD
Type
protein-coding
Description
Rieske Fe-S domain containing
Entrez Gene ID
317671
Genome
hg19
Position
chr5:94,982,593-94,992,837
Genome
hg38
Position
chr5:95,646,889-95,657,133
HGNC
HGNC:29587 HGNC
Ensembl
ENSG00000175449 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
16
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
HGNC HGNC:29587 HGNC
Ensembl ENSG00000175449 Ensembl
AllianceGenome HGNC:29587
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000380005.9 hg38 chr5 95,646,777 95,658,082 11,306
ENST00000458310.2 hg38 chr5 95,646,889 95,657,133 10,245
ENST00000511684.6 hg38 chr5 95,646,777 95,658,082 11,306
ENST00000311364.9 hg38 chr5 95,646,889 95,657,140 10,252
ENST00000513950.2 hg38 chr5 95,654,061 95,656,333 2,273
ENST00000380005.9 hg19 chr5 94,982,481 94,993,786 11,306
ENST00000511684.6 hg19 chr5 94,982,481 94,993,786 11,306
ENST00000458310.2 hg19 chr5 94,982,593 94,992,837 10,245
ENST00000311364.9 hg19 chr5 94,982,593 94,992,844 10,252
ENST00000513950.2 hg19 chr5 94,989,765 94,992,037 2,273
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