PARVG parvin gamma

Information
Symbol
PARVG
Type
protein-coding
Description
parvin gamma
Entrez Gene ID
64098
Genome
hg19
Position
chr22:44,576,805-44,604,349
Genome
hg38
Position
chr22:44,180,925-44,208,469
MIM
608122 OMIM
HGNC
HGNC:14654 HGNC
Ensembl
ENSG00000138964 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 1 0
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
46
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
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 608122 OMIM
HGNC HGNC:14654 HGNC
Ensembl ENSG00000138964 Ensembl
AllianceGenome HGNC:14654
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000466375.2 hg38 chr22 44,181,861 44,184,261 2,401
ENST00000444313.8 hg38 chr22 44,180,925 44,208,469 27,545
ENST00000422871.5 hg38 chr22 44,172,956 44,208,468 35,513
ENST00000422871.5 hg19 chr22 44,568,836 44,604,348 35,513
ENST00000444313.8 hg19 chr22 44,576,805 44,604,349 27,545
ENST00000466375.2 hg19 chr22 44,577,741 44,580,141 2,401
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