C12orf42-AS1 C12orf42 antisense RNA 1

Information
Symbol
C12orf42-AS1
Type
ncRNA
Description
C12orf42 antisense RNA 1
Entrez Gene ID
101929058
Genome
hg19
Position
chr12:103,545,612-103,573,025
Genome
hg38
Position
chr12:103,151,834-103,179,247
HGNC
HGNC:56185 HGNC
Ensembl
ENSG00000257860 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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:56185 HGNC
Ensembl ENSG00000257860 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000552759.1 hg38 chr12 103,151,855 103,161,642 9,788
ENST00000547418.5 hg38 chr12 103,151,842 103,168,234 16,393
ENST00000660400.1 hg38 chr12 103,156,184 103,178,263 22,080
ENST00000652849.1 hg38 chr12 103,151,834 103,178,264 26,431
ENST00000549568.5 hg38 chr12 103,162,856 103,168,309 5,454
ENST00000658970.1 hg38 chr12 103,151,834 103,179,247 27,414
ENST00000652849.1 hg19 chr12 103,545,612 103,572,042 26,431
ENST00000658970.1 hg19 chr12 103,545,612 103,573,025 27,414
ENST00000547418.5 hg19 chr12 103,545,620 103,562,012 16,393
ENST00000552759.1 hg19 chr12 103,545,633 103,555,420 9,788
ENST00000660400.1 hg19 chr12 103,549,962 103,572,041 22,080
ENST00000549568.5 hg19 chr12 103,556,634 103,562,087 5,454
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