MAGEB1 MAGE family member B1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 6 |
not provided | 6 | 0 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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44 |
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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
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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 |
Search Word
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 | CT3.1 |
SYNONYM | DAM10 |
SYNONYM | MAGE-Xp |
SYNONYM | MAGEL1 |
MIM | 300097 OMIM |
HGNC | HGNC:6808 HGNC |
Ensembl | ENSG00000214107 Ensembl |
AllianceGenome | HGNC:6808 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000378981.8 | hg38 | chrX | 30,243,715 | 30,252,038 | 8,324 |
ENST00000397550.6 | hg38 | chrX | 30,243,715 | 30,252,038 | 8,324 |
ENST00000397548.4 | hg38 | chrX | 30,247,146 | 30,252,040 | 4,895 |
ENST00000378981.8 | hg19 | chrX | 30,261,832 | 30,270,155 | 8,324 |
ENST00000397550.6 | hg19 | chrX | 30,261,832 | 30,270,155 | 8,324 |
ENST00000397548.4 | hg19 | chrX | 30,265,263 | 30,270,157 | 4,895 |
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