CCDC91 coiled-coil domain containing 91

Information
Symbol
CCDC91
Type
protein-coding
Description
coiled-coil domain containing 91
Entrez Gene ID
55297
Genome
hg19
Position
chr12:28,343,379-28,703,099
Genome
hg38
Position
chr12:28,190,446-28,550,166
MIM
617366 OMIM
HGNC
HGNC:24855 HGNC
Ensembl
ENSG00000123106 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
not provided 3 0
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
42
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
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 HSD8
SYNONYM p56
MIM 617366 OMIM
HGNC HGNC:24855 HGNC
Ensembl ENSG00000123106 Ensembl
AllianceGenome HGNC:24855
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000536442.6 hg38 chr12 28,190,456 28,550,166 359,711
ENST00000381259.5 hg38 chr12 28,257,200 28,550,165 292,966
ENST00000539107.5 hg38 chr12 28,190,427 28,550,166 359,740
ENST00000545336.5 hg38 chr12 28,190,446 28,550,166 359,721
ENST00000539107.5 hg19 chr12 28,343,360 28,703,099 359,740
ENST00000545336.5 hg19 chr12 28,343,379 28,703,099 359,721
ENST00000536442.6 hg19 chr12 28,343,389 28,703,099 359,711
ENST00000381259.5 hg19 chr12 28,410,133 28,703,098 292,966
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