C6orf132 chromosome 6 open reading frame 132

Information
Symbol
C6orf132
Type
protein-coding
Description
chromosome 6 open reading frame 132
Entrez Gene ID
647024
Genome
hg19
Position
chr6:42,068,857-42,110,358
Genome
hg38
Position
chr6:42,101,119-42,142,620
MIM
620839 OMIM
HGNC
HGNC:21288 HGNC
Ensembl
ENSG00000188112 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 36
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
SYNONYM LncCCLM
SYNONYM bA7K24.2
MIM 620839 OMIM
HGNC HGNC:21288 HGNC
Ensembl ENSG00000188112 Ensembl
AllianceGenome HGNC:21288
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000356542.5 hg38 chr6 42,126,377 42,142,619 16,243
ENST00000341865.9 hg38 chr6 42,101,119 42,142,620 41,502
ENST00000341865.9 hg19 chr6 42,068,857 42,110,358 41,502
ENST00000356542.5 hg19 chr6 42,094,115 42,110,357 16,243
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