CCDC77 coiled-coil domain containing 77

Information
Symbol
CCDC77
Type
protein-coding
Description
coiled-coil domain containing 77
Entrez Gene ID
84318
Genome
hg19
Position
chr12:510,810-551,808
Genome
hg38
Position
chr12:401,644-442,642
HGNC
HGNC:28203 HGNC
Ensembl
ENSG00000120647 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 2 0
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
58
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
HGNC HGNC:28203 HGNC
Ensembl ENSG00000120647 Ensembl
AllianceGenome HGNC:28203
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000412006.6 hg38 chr12 401,637 442,642 41,006
ENST00000540180.5 hg38 chr12 389,348 442,004 52,657
ENST00000239830.9 hg38 chr12 401,644 442,642 40,999
ENST00000422000.5 hg38 chr12 389,350 442,638 53,289
ENST00000540180.5 hg19 chr12 498,514 551,170 52,657
ENST00000422000.5 hg19 chr12 498,516 551,804 53,289
ENST00000412006.6 hg19 chr12 510,803 551,808 41,006
ENST00000239830.9 hg19 chr12 510,810 551,808 40,999
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