SEC14L4 SEC14 like lipid binding 4

Information
Symbol
SEC14L4
Type
protein-coding
Description
SEC14 like lipid binding 4
Entrez Gene ID
284904
Genome
hg19
Position
chr22:30,884,889-30,901,682
Genome
hg38
Position
chr22:30,488,902-30,505,695
MIM
612825 OMIM
HGNC
HGNC:20627 HGNC
Ensembl
ENSG00000133488 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
52
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 TAP3
MIM 612825 OMIM
HGNC HGNC:20627 HGNC
Ensembl ENSG00000133488 Ensembl
AllianceGenome HGNC:20627
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000381982.3 hg38 chr22 30,489,396 30,505,650 16,255
ENST00000255858.12 hg38 chr22 30,488,902 30,505,695 16,794
ENST00000255858.12 hg19 chr22 30,884,889 30,901,682 16,794
ENST00000381982.3 hg19 chr22 30,885,383 30,901,637 16,255
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