SLC16A14 solute carrier family 16 member 14

Information
Symbol
SLC16A14
Type
protein-coding
Description
solute carrier family 16 member 14
Entrez Gene ID
151473
Genome
hg19
Position
chr2:230,899,698-230,933,640
Genome
hg38
Position
chr2:230,034,982-230,068,924
HGNC
HGNC:26417 HGNC
Ensembl
ENSG00000163053 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
42
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 MCT14
HGNC HGNC:26417 HGNC
Ensembl ENSG00000163053 Ensembl
AllianceGenome HGNC:26417
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000295190.9 hg38 chr2 230,034,982 230,068,924 33,943
ENST00000295190.9 hg19 chr2 230,899,698 230,933,640 33,943
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