MAGEA6 MAGE family member A6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 3 |
not provided | 6 | 0 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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1 |
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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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 |
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Target data | : |
MGeND data only
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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 | CT1.6 |
SYNONYM | MAGE-3b |
SYNONYM | MAGE3B |
SYNONYM | MAGE6 |
MIM | 300176 OMIM |
HGNC | HGNC:6804 HGNC |
Ensembl | ENSG00000197172 Ensembl |
AllianceGenome | HGNC:6804 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000616035.4 | hg38 | chrX | 152,766,147 | 152,769,716 | 3,570 |
ENST00000329342.10 | hg38 | chrX | 152,766,136 | 152,769,689 | 3,554 |
ENST00000329342.5 | hg19 | chrX | 151,867,214 | 151,870,825 | 3,612 |
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