VRTN vertebrae development associated

Information
Symbol
VRTN
Type
protein-coding
Description
vertebrae development associated
Entrez Gene ID
55237
Genome
hg19
Position
chr14:74,815,174-74,826,711
Genome
hg38
Position
chr14:74,348,471-74,360,008
MIM
620468 OMIM
HGNC
HGNC:20223 HGNC
Ensembl
ENSG00000133980 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
72
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 :
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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 C14orf115
SYNONYM vertnin
MIM 620468 OMIM
HGNC HGNC:20223 HGNC
Ensembl ENSG00000133980 Ensembl
AllianceGenome HGNC:20223
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000256362.5 hg38 chr14 74,348,471 74,360,008 11,538
ENST00000256362.5 hg19 chr14 74,815,174 74,826,711 11,538
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