C12orf75 chromosome 12 open reading frame 75

Information
Symbol
C12orf75
Type
protein-coding
Description
chromosome 12 open reading frame 75
Entrez Gene ID
387882
Genome
hg19
Position
chr12:105,724,469-105,765,296
Genome
hg38
Position
chr12:105,330,691-105,371,518
HGNC
HGNC:35164 HGNC
Ensembl
ENSG00000235162 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 4
Ranking
ClinVar
0
0
0
4
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 AGD3
SYNONYM OCC-1
SYNONYM OCC1
HGNC HGNC:35164 HGNC
Ensembl ENSG00000235162 Ensembl
AllianceGenome HGNC:35164
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000552457.1 hg38 chr12 105,330,674 105,370,940 40,267
ENST00000612117.4 hg38 chr12 105,330,636 105,371,517 40,882
ENST00000443585.6 hg38 chr12 105,330,691 105,371,518 40,828
ENST00000549893.5 hg38 chr12 105,330,710 105,396,097 65,388
ENST00000612117.4 hg19 chr12 105,724,414 105,765,295 40,882
ENST00000552457.1 hg19 chr12 105,724,452 105,764,718 40,267
ENST00000443585.6 hg19 chr12 105,724,469 105,765,296 40,828
ENST00000549893.5 hg19 chr12 105,724,488 105,789,875 65,388
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