MAGED2 MAGE family member D2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 10 |
Likely pathogenic | 0 | 10 |
Benign | 0 | 74 |
Likely benign | 0 | 40 |
Conflicting classifications of pathogenicity | 0 | 4 |
not provided | 6 | 0 |
Uncertain significance | 0 | 86 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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22 |
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182 |
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8 |
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 |
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 | 11B6 |
SYNONYM | BARTS5 |
SYNONYM | BCG-1 |
SYNONYM | BCG1 |
SYNONYM | HCA10 |
SYNONYM | MAGE-D2 |
MIM | 300470 OMIM |
HGNC | HGNC:16353 HGNC |
Ensembl | ENSG00000102316 Ensembl |
AllianceGenome | HGNC:16353 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000627068.2 | hg38 | chrX | 54,807,599 | 54,815,694 | 8,096 |
ENST00000375053.6 | hg38 | chrX | 54,807,599 | 54,815,694 | 8,096 |
ENST00000218439.8 | hg38 | chrX | 54,808,338 | 54,815,694 | 7,357 |
ENST00000347546.8 | hg38 | chrX | 54,807,747 | 54,816,007 | 8,261 |
ENST00000375058.5 | hg38 | chrX | 54,808,371 | 54,816,007 | 7,637 |
ENST00000375060.5 | hg38 | chrX | 54,808,371 | 54,816,012 | 7,642 |
ENST00000396224.1 | hg38 | chrX | 54,809,060 | 54,815,694 | 6,635 |
ENST00000375068.6 | hg38 | chrX | 54,807,745 | 54,816,015 | 8,271 |
ENST00000375053.6 | hg19 | chrX | 54,834,032 | 54,842,127 | 8,096 |
ENST00000627068.2 | hg19 | chrX | 54,834,032 | 54,842,127 | 8,096 |
ENST00000375068.6 | hg19 | chrX | 54,834,178 | 54,842,448 | 8,271 |
ENST00000347546.8 | hg19 | chrX | 54,834,180 | 54,842,440 | 8,261 |
ENST00000218439.8 | hg19 | chrX | 54,834,771 | 54,842,127 | 7,357 |
ENST00000375058.5 | hg19 | chrX | 54,834,804 | 54,842,440 | 7,637 |
ENST00000375060.5 | hg19 | chrX | 54,834,804 | 54,842,445 | 7,642 |
ENST00000396224.1 | hg19 | chrX | 54,835,493 | 54,842,127 | 6,635 |
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