H2BC8 H2B clustered histone 8
Clinical Significance
MGeND | ClinVar | |
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not provided | 2 | 0 |
Uncertain significance | 0 | 7 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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7 |
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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 | : |
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 | H2B.1A |
SYNONYM | H2B/a |
SYNONYM | H2BC10 |
SYNONYM | H2BC4 |
SYNONYM | H2BC6 |
SYNONYM | H2BC7 |
SYNONYM | H2BFA |
SYNONYM | HIST1H2BG |
SYNONYM | dJ221C16.8 |
MIM | 602798 OMIM |
HGNC | HGNC:4746 HGNC |
Ensembl | ENSG00000273802 Ensembl |
AllianceGenome | HGNC:4746 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000541790.4 | hg38 | chr6 | 26,216,200 | 26,216,688 | 489 |
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