H2AX H2A.X variant histone
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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6 |
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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
[No Data.]
Locus Zoom
Variants
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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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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 | H2A.X |
SYNONYM | H2A/X |
SYNONYM | H2AFX |
MIM | 601772 OMIM |
HGNC | HGNC:4739 HGNC |
Ensembl | ENSG00000188486 Ensembl |
AllianceGenome | HGNC:4739 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000530167.2 | hg38 | chr11 | 119,093,874 | 119,095,465 | 1,592 |
ENST00000530167.2 | hg19 | chr11 | 118,964,584 | 118,966,175 | 1,592 |
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