CD14 CD14 molecule

Information
Symbol
CD14
Type
protein-coding
Description
CD14 molecule
Entrez Gene ID
929
Genome
hg19
Position
chr5:140,011,313-140,013,285
Genome
hg38
Position
chr5:140,631,728-140,633,700
MIM
158120 OMIM
HGNC
HGNC:1628 HGNC
Ensembl
ENSG00000170458 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 6
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
46
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
MIM 158120 OMIM
HGNC HGNC:1628 HGNC
Ensembl ENSG00000170458 Ensembl
AllianceGenome HGNC:1628
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000302014.11 hg38 chr5 140,631,732 140,633,175 1,444
ENST00000498971.7 hg38 chr5 140,631,728 140,633,651 1,924
ENST00000512545.2 hg38 chr5 140,631,728 140,633,700 1,973
ENST00000519715.2 hg38 chr5 140,631,728 140,633,672 1,945
ENST00000498971.7 hg19 chr5 140,011,313 140,013,236 1,924
ENST00000519715.2 hg19 chr5 140,011,313 140,013,257 1,945
ENST00000512545.2 hg19 chr5 140,011,313 140,013,285 1,973
ENST00000302014.11 hg19 chr5 140,011,317 140,012,760 1,444
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