C6orf136 chromosome 6 open reading frame 136

Information
Symbol
C6orf136
Type
protein-coding
Description
chromosome 6 open reading frame 136
Entrez Gene ID
221545
Genome
hg19
Position
chr6:30,614,910-30,620,984
Genome
hg38
Position
chr6:30,647,133-30,653,207
HGNC
HGNC:21301 HGNC
Ensembl
ENSG00000204564 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
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
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:21301 HGNC
Ensembl ENSG00000204564 Ensembl
AllianceGenome HGNC:21301
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000293604.10 hg38 chr6 30,647,039 30,653,209 6,171
ENST00000376473.9 hg38 chr6 30,647,073 30,653,210 6,138
ENST00000376471.8 hg38 chr6 30,647,164 30,652,915 5,752
ENST00000651131.1 hg38 chr6 30,647,133 30,653,207 6,075
ENST00000293604.10 hg19 chr6 30,614,816 30,620,986 6,171
ENST00000376473.9 hg19 chr6 30,614,850 30,620,987 6,138
ENST00000651131.1 hg19 chr6 30,614,910 30,620,984 6,075
ENST00000376471.8 hg19 chr6 30,614,941 30,620,692 5,752
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