H2AC1 H2A clustered histone 1
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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 |
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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 | H2AA |
SYNONYM | H2AFR |
SYNONYM | HIST1H2AA |
SYNONYM | HISTH2AA |
SYNONYM | TH2A |
SYNONYM | bA317E16.2 |
MIM | 613499 OMIM |
HGNC | HGNC:18729 HGNC |
Ensembl | ENSG00000164508 Ensembl |
AllianceGenome | HGNC:18729 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000297012.5 | hg38 | chr6 | 25,726,063 | 25,726,562 | 500 |
ENST00000297012.5 | hg19 | chr6 | 25,726,291 | 25,726,790 | 500 |
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