C11orf91 chromosome 11 open reading frame 91

Information
Symbol
C11orf91
Type
protein-coding
Description
chromosome 11 open reading frame 91
Entrez Gene ID
100131378
Genome
hg19
Position
chr11:33,719,807-33,722,372
Genome
hg38
Position
chr11:33,698,261-33,700,826
HGNC
HGNC:34444 HGNC
Ensembl
ENSG00000205177 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 6
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
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:34444 HGNC
Ensembl ENSG00000205177 Ensembl
AllianceGenome HGNC:34444
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000379011.5 hg38 chr11 33,698,261 33,700,826 2,566
ENST00000379011.5 hg19 chr11 33,719,807 33,722,372 2,566
Genome browser