MAGEA2B MAGE family member A2B
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| 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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CT1.2 |
| SYNONYM | MAGE2 |
| MIM | 300549 OMIM |
| HGNC | HGNC:19340 HGNC |
| Ensembl | ENSG00000183305 Ensembl |
| AllianceGenome | HGNC:19340 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000331220.6 | hg38 | chrX | 152,714,586 | 152,718,606 | 4,021 |
| ENST00000682532.1 | hg38 | chrX | 152,714,628 | 152,718,607 | 3,980 |
| ENST00000370293.6 | hg38 | chrX | 152,714,601 | 152,718,607 | 4,007 |
| ENST00000331220.6 | hg19 | chrX | 151,883,075 | 151,887,095 | 4,021 |
| ENST00000370293.6 | hg19 | chrX | 151,883,090 | 151,887,096 | 4,007 |
| ENST00000682532.1 | hg19 | chrX | 151,883,117 | 151,887,096 | 3,980 |
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