EVI2B ecotropic viral integration site 2B

Information
Symbol
EVI2B
Type
protein-coding
Description
ecotropic viral integration site 2B
Entrez Gene ID
2124
Genome
hg19
Position
chr17:29,630,788-29,641,072
Genome
hg38
Position
chr17:31,303,770-31,314,054
MIM
158381 OMIM
HGNC
HGNC:3500 HGNC
Ensembl
ENSG00000185862 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 14
Conflicting classifications of pathogenicity 0 2
not provided 4 0
Uncertain significance 0 62
Ranking
ClinVar
0
0
6
76
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
SYNONYM CD361
SYNONYM D17S376
SYNONYM EVDB
MIM 158381 OMIM
HGNC HGNC:3500 HGNC
Ensembl ENSG00000185862 Ensembl
AllianceGenome HGNC:3500
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577894.1 hg38 chr17 31,304,234 31,314,105 9,872
ENST00000330927.5 hg38 chr17 31,303,770 31,314,054 10,285
ENST00000330927.5 hg19 chr17 29,630,788 29,641,072 10,285
ENST00000577894.1 hg19 chr17 29,631,252 29,641,123 9,872
KeyValue
strand-
UniProtOG
start29,630,787
Gene SymbolEVI2B
Entrez GeneId2,124
Chr Band17q11.2
end29,641,129
chrchr17
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