C11orf68 chromosome 11 open reading frame 68

Information
Symbol
C11orf68
Type
protein-coding
Description
chromosome 11 open reading frame 68
Entrez Gene ID
83638
Genome
hg19
Position
chr11:65,684,281-65,686,533
Genome
hg38
Position
chr11:65,916,810-65,919,062
HGNC
HGNC:28801 HGNC
Ensembl
ENSG00000175573 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
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
SYNONYM BLES03
SYNONYM P5326
HGNC HGNC:28801 HGNC
Ensembl ENSG00000175573 Ensembl
AllianceGenome HGNC:28801
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000438576.3 hg38 chr11 65,916,810 65,919,062 2,253
ENST00000449692.3 hg38 chr11 65,916,810 65,919,062 2,253
ENST00000530188.1 hg38 chr11 65,916,833 65,918,360 1,528
ENST00000438576.3 hg19 chr11 65,684,281 65,686,533 2,253
ENST00000449692.3 hg19 chr11 65,684,281 65,686,533 2,253
ENST00000530188.1 hg19 chr11 65,684,304 65,685,831 1,528
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