MAGEB2 MAGE family member B2

Information
Symbol
MAGEB2
Type
protein-coding
Description
MAGE family member B2
Entrez Gene ID
4113
Genome
hg19
Position
chrX:30,233,680-30,238,206
Genome
hg38
Position
chrX:30,215,563-30,220,089
MIM
300098 OMIM
HGNC
HGNC:6809 HGNC
Ensembl
ENSG00000099399 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 12
Conflicting classifications of pathogenicity 0 2
not provided 6 0
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
44
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 CT3.2
SYNONYM DAM6
SYNONYM MAGE-XP-2
MIM 300098 OMIM
HGNC HGNC:6809 HGNC
Ensembl ENSG00000099399 Ensembl
AllianceGenome HGNC:6809
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000378988.5 hg38 chrX 30,215,563 30,220,089 4,527
ENST00000378988.5 hg19 chrX 30,233,680 30,238,206 4,527
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