C2orf68 chromosome 2 open reading frame 68

Information
Symbol
C2orf68
Type
protein-coding
Description
chromosome 2 open reading frame 68
Entrez Gene ID
388969
Genome
hg19
Position
chr2:85,832,377-85,839,189
Genome
hg38
Position
chr2:85,605,254-85,612,066
MIM
618519 OMIM
HGNC
HGNC:34353 HGNC
Ensembl
ENSG00000168887 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 HCRCN81
MIM 618519 OMIM
HGNC HGNC:34353 HGNC
Ensembl ENSG00000168887 Ensembl
AllianceGenome HGNC:34353
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409734.3 hg38 chr2 85,610,220 85,612,032 1,813
ENST00000306336.6 hg38 chr2 85,605,254 85,612,066 6,813
ENST00000306336.6 hg19 chr2 85,832,377 85,839,189 6,813
ENST00000409734.3 hg19 chr2 85,837,343 85,839,155 1,813
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