C12orf42 chromosome 12 open reading frame 42

Information
Symbol
C12orf42
Type
protein-coding
Description
chromosome 12 open reading frame 42
Entrez Gene ID
374470
Genome
hg19
Position
chr12:103,695,733-103,889,756
Genome
hg38
Position
chr12:103,301,955-103,495,978
HGNC
HGNC:24729 HGNC
Ensembl
ENSG00000179088 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 4
Ranking
ClinVar
0
0
0
6
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:24729 HGNC
Ensembl ENSG00000179088 Ensembl
AllianceGenome HGNC:24729
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000378113.7 hg38 chr12 103,301,955 103,495,978 194,024
ENST00000548883.6 hg38 chr12 103,301,955 103,495,968 194,014
ENST00000548048.5 hg38 chr12 103,301,955 103,495,966 194,012
ENST00000548048.5 hg19 chr12 103,695,733 103,889,744 194,012
ENST00000548883.6 hg19 chr12 103,695,733 103,889,746 194,014
ENST00000378113.7 hg19 chr12 103,695,733 103,889,756 194,024
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