C16orf92 chromosome 16 open reading frame 92

Information
Symbol
C16orf92
Type
protein-coding
Description
chromosome 16 open reading frame 92
Entrez Gene ID
146378
Genome
hg19
Position
chr16:30,034,655-30,036,023
Genome
hg38
Position
chr16:30,023,334-30,024,702
MIM
618911 OMIM
HGNC
HGNC:26346 HGNC
Ensembl
ENSG00000167194 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 9 0
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
2
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
SYNONYM FIMP
MIM 618911 OMIM
HGNC HGNC:26346 HGNC
Ensembl ENSG00000167194 Ensembl
AllianceGenome HGNC:26346
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000300575.6 hg38 chr16 30,023,334 30,024,702 1,369
ENST00000681219.1 hg38 chr16 30,023,198 30,024,704 1,507
ENST00000681219.1 hg19 chr16 30,034,519 30,036,025 1,507
ENST00000300575.6 hg19 chr16 30,034,655 30,036,023 1,369
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