CT45A6 cancer/testis antigen family 45 member A6
Clinical Significance
MGeND | ClinVar | |
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not provided | 6 | 0 |
Uncertain significance | 0 | 2 |
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
Disease area statistics
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Variants
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Target data | : |
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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 | CT45-5 |
SYNONYM | CT45-6 |
SYNONYM | CT45.6 |
SYNONYM | CT45A5 |
SYNONYM | CT45A7 |
MIM | 300797 OMIM |
HGNC | HGNC:33271 HGNC |
Ensembl | ENSG00000278289 Ensembl |
AllianceGenome | HGNC:33271 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000620654.2 | hg38 | chrX | 135,794,685 | 135,802,787 | 8,103 |
ENST00000612878.4 | hg38 | chrX | 135,794,706 | 135,799,001 | 4,296 |
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