MAGEB5 MAGE family member B5
Clinical Significance
MGeND | ClinVar | |
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not provided | 6 | 0 |
Ranking
ClinVar | |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CT3.3 |
SYNONYM | MAGE-B5 |
MIM | 300466 OMIM |
HGNC | HGNC:23795 HGNC |
Ensembl | ENSG00000188408 Ensembl |
AllianceGenome | HGNC:23795 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000602297.1 | hg38 | chrX | 26,216,169 | 26,218,270 | 2,102 |
ENST00000602297.1 | hg19 | chrX | 26,234,286 | 26,236,387 | 2,102 |
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