SEMA4G semaphorin 4G

Information
Symbol
SEMA4G
Type
protein-coding
Description
semaphorin 4G
Entrez Gene ID
57715
Genome
hg19
Position
chr10:102,729,261-102,745,373
Genome
hg38
Position
chr10:100,969,504-100,985,616
MIM
618991 OMIM
HGNC
HGNC:10735 HGNC
Ensembl
ENSG00000095539 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 4
Uncertain significance 0 122
Ranking
ClinVar
0
0
0
136
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 618991 OMIM
HGNC HGNC:10735 HGNC
Ensembl ENSG00000095539 Ensembl
AllianceGenome HGNC:10735
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000370250.8 hg38 chr10 100,972,540 100,984,837 12,298
ENST00000517724.5 hg38 chr10 100,972,712 100,985,258 12,547
ENST00000210633.4 hg38 chr10 100,969,504 100,985,616 16,113
ENST00000210633.4 hg19 chr10 102,729,261 102,745,373 16,113
ENST00000370250.8 hg19 chr10 102,732,297 102,744,594 12,298
ENST00000517724.5 hg19 chr10 102,732,469 102,745,015 12,547
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