H2AC6 H2A clustered histone 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
not provided | 10 | 0 |
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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8 |
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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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Target data | : |
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 | H2A/l |
SYNONYM | H2AFL |
SYNONYM | HIST1H2AC |
SYNONYM | dJ221C16.4 |
MIM | 602794 OMIM |
HGNC | HGNC:4733 HGNC |
Ensembl | ENSG00000180573 Ensembl |
AllianceGenome | HGNC:4733 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000377791.4 | hg38 | chr6 | 26,124,172 | 26,124,690 | 519 |
ENST00000602637.1 | hg38 | chr6 | 26,124,203 | 26,139,084 | 14,882 |
ENST00000377791.4 | hg19 | chr6 | 26,124,400 | 26,124,918 | 519 |
ENST00000602637.1 | hg19 | chr6 | 26,124,431 | 26,139,312 | 14,882 |
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