GAGE12F G antigen 12F
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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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Filtering | : |
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 | AL4 |
SYNONYM | CT4.7 |
SYNONYM | GAGE-7 |
SYNONYM | GAGE-7B |
SYNONYM | GAGE-8 |
SYNONYM | GAGE7 |
SYNONYM | GAGE7B |
MIM | 300730 OMIM |
HGNC | HGNC:31906 HGNC |
Ensembl | ENSG00000236362 Ensembl |
AllianceGenome | HGNC:31906 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000440137.2 | hg38 | chrX | 49,560,842 | 49,568,205 | 7,364 |
ENST00000639028.1 | hg38 | chrX | 49,551,278 | 49,568,218 | 16,941 |
ENST00000639028.1 | hg19 | chrX | 49,315,881 | 49,332,821 | 16,941 |
ENST00000440137.2 | hg19 | chrX | 49,325,445 | 49,332,808 | 7,364 |
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