CFAP97D2 CFAP97 domain containing 2

Information
Symbol
CFAP97D2
Type
protein-coding
Description
CFAP97 domain containing 2
Entrez Gene ID
101929355
Genome
hg19
Position
chr13:114,944,725-114,988,559
Genome
hg38
Position
chr13:114,179,250-114,223,084
HGNC
HGNC:53789 HGNC
Ensembl
ENSG00000283361 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
HGNC HGNC:53789 HGNC
Ensembl ENSG00000283361 Ensembl
AllianceGenome HGNC:53789
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000635901.2 hg38 chr13 114,179,250 114,223,084 43,835
ENST00000646158.1 hg38 chr13 114,179,331 114,222,518 43,188
ENST00000636692.2 hg38 chr13 114,179,257 114,223,085 43,829
ENST00000635901.2 hg19 chr13 114,944,725 114,988,559 43,835
ENST00000636692.2 hg19 chr13 114,944,732 114,988,560 43,829
ENST00000646158.1 hg19 chr13 114,944,806 114,987,993 43,188
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