H2AC8 H2A clustered histone 8
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
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 |
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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 | H2A.1 |
SYNONYM | H2A.2 |
SYNONYM | H2A/a |
SYNONYM | H2AC4 |
SYNONYM | H2AFA |
SYNONYM | HIST1H2AE |
MIM | 602786 OMIM |
HGNC | HGNC:4724 HGNC |
Ensembl | ENSG00000277075 Ensembl |
AllianceGenome | HGNC:4724 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000303910.5 | hg38 | chr6 | 26,216,921 | 26,217,437 | 517 |
ENST00000303910.5 | hg19 | chr6 | 26,217,149 | 26,217,665 | 517 |
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