VIL1 villin 1

Information
Symbol
VIL1
Type
protein-coding
Description
villin 1
Entrez Gene ID
7429
Genome
hg19
Position
chr2:219,283,846-219,318,018
Genome
hg38
Position
chr2:218,419,123-218,453,295
MIM
193040 OMIM
HGNC
HGNC:12690 HGNC
Ensembl
ENSG00000127831 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 24
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 92
Ranking
ClinVar
0
0
0
128
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 :
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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 D2S1471
SYNONYM VIL
MIM 193040 OMIM
HGNC HGNC:12690 HGNC
Ensembl ENSG00000127831 Ensembl
AllianceGenome HGNC:12690
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000248444.10 hg38 chr2 218,419,123 218,453,295 34,173
ENST00000440053.1 hg38 chr2 218,423,765 218,431,216 7,452
ENST00000392114.6 hg38 chr2 218,419,123 218,449,524 30,402
ENST00000392114.6 hg19 chr2 219,283,846 219,314,247 30,402
ENST00000248444.10 hg19 chr2 219,283,846 219,318,018 34,173
ENST00000440053.1 hg19 chr2 219,288,488 219,295,939 7,452
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