VNN2 vanin 2

Information
Symbol
VNN2
Type
protein-coding
Description
vanin 2
Entrez Gene ID
8875
Genome
hg19
Position
chr6:133,065,009-133,079,043
Genome
hg38
Position
chr6:132,743,870-132,757,904
MIM
603571 OMIM
HGNC
HGNC:12706 HGNC
Ensembl
ENSG00000112303 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 8
Uncertain significance 0 56
Ranking
ClinVar
0
0
0
68
2
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 :
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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 FOAP-4
SYNONYM GPI-80
MIM 603571 OMIM
HGNC HGNC:12706 HGNC
Ensembl ENSG00000112303 Ensembl
AllianceGenome HGNC:12706
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000326499.11 hg38 chr6 132,743,870 132,757,904 14,035
ENST00000525270.5 hg38 chr6 132,744,196 132,763,447 19,252
ENST00000525289.5 hg38 chr6 132,744,300 132,757,883 13,584
ENST00000326499.11 hg19 chr6 133,065,009 133,079,043 14,035
ENST00000525270.5 hg19 chr6 133,065,335 133,084,586 19,252
ENST00000525289.5 hg19 chr6 133,065,439 133,079,022 13,584
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