VILL villin like

Information
Symbol
VILL
Type
protein-coding
Description
villin like
Entrez Gene ID
50853
Genome
hg19
Position
chr3:38,029,550-38,048,679
Genome
hg38
Position
chr3:37,988,059-38,007,188
MIM
619666 OMIM
HGNC
HGNC:30906 HGNC
Ensembl
ENSG00000136059 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 14
Uncertain significance 0 114
Ranking
ClinVar
0
0
0
130
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
MIM 619666 OMIM
HGNC HGNC:30906 HGNC
Ensembl ENSG00000136059 Ensembl
AllianceGenome HGNC:30906
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000465644.5 hg38 chr3 37,994,153 38,007,161 13,009
ENST00000383759.7 hg38 chr3 37,990,786 38,007,185 16,400
ENST00000283713.10 hg38 chr3 37,988,059 38,007,188 19,130
ENST00000283713.10 hg19 chr3 38,029,550 38,048,679 19,130
ENST00000383759.7 hg19 chr3 38,032,277 38,048,676 16,400
ENST00000465644.5 hg19 chr3 38,035,644 38,048,652 13,009
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