C12orf60 chromosome 12 open reading frame 60

Information
Symbol
C12orf60
Type
protein-coding
Description
chromosome 12 open reading frame 60
Entrez Gene ID
144608
Genome
hg19
Position
chr12:14,956,604-14,977,349
Genome
hg38
Position
chr12:14,803,670-14,824,415
HGNC
HGNC:28726 HGNC
Ensembl
ENSG00000182993 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 40
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
[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
HGNC HGNC:28726 HGNC
Ensembl ENSG00000182993 Ensembl
AllianceGenome HGNC:28726
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000330828.3 hg38 chr12 14,803,670 14,824,415 20,746
ENST00000330828.3 hg19 chr12 14,956,604 14,977,349 20,746
Genome browser