CCL14 C-C motif chemokine ligand 14

Information
Symbol
CCL14
Type
protein-coding
Description
C-C motif chemokine ligand 14
Entrez Gene ID
6358
Genome
hg19
Position
chr17:34,310,695-34,313,685
Genome
hg38
Position
chr17:35,983,659-35,986,649
MIM
601392 OMIM
HGNC
HGNC:10612 HGNC
Ensembl
ENSG00000276409 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
8
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 CC-1
SYNONYM CC-3
SYNONYM CKB1
SYNONYM HCC-1
SYNONYM HCC-1(1-74)
SYNONYM HCC-1/HCC-3
SYNONYM HCC-3
SYNONYM MCIF
SYNONYM NCC-2
SYNONYM NCC2
SYNONYM SCYA14
SYNONYM SCYL2
SYNONYM SY14
MIM 601392 OMIM
HGNC HGNC:10612 HGNC
Ensembl ENSG00000276409 Ensembl
AllianceGenome HGNC:10612
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000618404.5 hg38 chr17 35,983,288 35,986,729 3,442
ENST00000622526.1 hg38 chr17 35,983,659 35,986,649 2,991
ENST00000614009.1 hg38 chr17 35,983,291 35,987,004 3,714
ENST00000620991.1 hg38 chr17 35,983,687 35,986,675 2,989
ENST00000618404.5 hg19 chr17 34,310,324 34,313,765 3,442
ENST00000614009.1 hg19 chr17 34,310,327 34,314,040 3,714
ENST00000622526.1 hg19 chr17 34,310,695 34,313,685 2,991
ENST00000620991.1 hg19 chr17 34,310,723 34,313,711 2,989
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