H2BC12 H2B clustered histone 12
Clinical Significance
MGeND | ClinVar | |
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not provided | 1 | 0 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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
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 |
Search Word
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 | H2B/S |
SYNONYM | H2BFAiii |
SYNONYM | H2BFT |
SYNONYM | H2BK |
SYNONYM | HIST1H2BK |
MIM | 615045 OMIM |
HGNC | HGNC:13954 HGNC |
Ensembl | ENSG00000197903 Ensembl |
AllianceGenome | HGNC:13954 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000356950.2 | hg38 | chr6 | 27,146,361 | 27,146,855 | 495 |
ENST00000356950.2 | hg19 | chr6 | 27,114,140 | 27,114,634 | 495 |
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