C15orf48 chromosome 15 open reading frame 48

Information
Symbol
C15orf48
Type
protein-coding
Description
chromosome 15 open reading frame 48
Entrez Gene ID
84419
Genome
hg19
Position
chr15:45,722,805-45,725,647
Genome
hg38
Position
chr15:45,430,607-45,433,449
MIM
608409 OMIM
HGNC
HGNC:29898 HGNC
Ensembl
ENSG00000166920 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
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
[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 COXFA4L3
SYNONYM FOAP-11
SYNONYM MIR147BHG
SYNONYM MISTRAV
SYNONYM MOCCI
SYNONYM NMES1
MIM 608409 OMIM
HGNC HGNC:29898 HGNC
Ensembl ENSG00000166920 Ensembl
AllianceGenome HGNC:29898
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000344300.3 hg38 chr15 45,430,607 45,433,449 2,843
ENST00000396650.7 hg38 chr15 45,430,610 45,433,340 2,731
ENST00000344300.3 hg19 chr15 45,722,805 45,725,647 2,843
ENST00000396650.7 hg19 chr15 45,722,808 45,725,538 2,731
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