C14orf180 chromosome 14 open reading frame 180

Information
Symbol
C14orf180
Type
protein-coding
Description
chromosome 14 open reading frame 180
Entrez Gene ID
400258
Genome
hg19
Position
chr14:105,046,101-105,055,880
Genome
hg38
Position
chr14:104,579,764-104,589,543
MIM
619392 OMIM
HGNC
HGNC:33795 HGNC
Ensembl
ENSG00000184601 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 C14orf77
SYNONYM NRAC
MIM 619392 OMIM
HGNC HGNC:33795 HGNC
Ensembl ENSG00000184601 Ensembl
AllianceGenome HGNC:33795
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000331952.6 hg38 chr14 104,579,764 104,589,543 9,780
ENST00000557649.6 hg38 chr14 104,579,764 104,590,515 10,752
ENST00000410013.1 hg38 chr14 104,581,141 104,589,808 8,668
ENST00000331952.6 hg19 chr14 105,046,101 105,055,880 9,780
ENST00000557649.6 hg19 chr14 105,046,101 105,056,852 10,752
ENST00000410013.1 hg19 chr14 105,047,478 105,056,145 8,668
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