CYCS cytochrome c, somatic

Information
Symbol
CYCS
Type
protein-coding
Description
cytochrome c, somatic
Entrez Gene ID
54205
Genome
hg19
Position
chr7:25,158,275-25,164,879
Genome
hg38
Position
chr7:25,118,656-25,125,260
MIM
123970 OMIM
HGNC
HGNC:19986 HGNC
Ensembl
ENSG00000172115 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 1 6
Likely pathogenic 0 12
Benign 2 2
Likely benign 0 30
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 54
Ranking
ClinVar
0
0
10
78
14
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 CYC
SYNONYM HCS
SYNONYM THC4
MIM 123970 OMIM
HGNC HGNC:19986 HGNC
Ensembl ENSG00000172115 Ensembl
AllianceGenome HGNC:19986
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409764.5 hg38 chr7 25,123,444 25,125,260 1,817
ENST00000409409.5 hg38 chr7 25,123,307 25,125,249 1,943
ENST00000305786.7 hg38 chr7 25,118,656 25,125,260 6,605
ENST00000305786.7 hg19 chr7 25,158,275 25,164,879 6,605
ENST00000409409.5 hg19 chr7 25,162,926 25,164,868 1,943
ENST00000409764.5 hg19 chr7 25,163,063 25,164,879 1,817
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