H3-3B H3.3 histone B
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 12 |
| Likely pathogenic | 0 | 22 |
| Benign | 0 | 6 |
| Conflicting classifications of pathogenicity | 0 | 4 |
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
2 |
 |
36 |
 |
12 |
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
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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 |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | BRYLIB2 |
| SYNONYM | H3-3A |
| SYNONYM | H3.3B |
| SYNONYM | H3F3B |
| MIM | 601058 OMIM |
| HGNC | HGNC:4765 HGNC |
| Ensembl | ENSG00000132475 Ensembl |
| AllianceGenome | HGNC:4765 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000586607.5 | hg38 | chr17 | 75,778,576 | 75,785,486 | 6,911 |
| ENST00000589599.5 | hg38 | chr17 | 75,778,574 | 75,779,780 | 1,207 |
| ENST00000254810.8 | hg38 | chr17 | 75,776,434 | 75,779,779 | 3,346 |
| ENST00000592643.5 | hg38 | chr17 | 75,778,250 | 75,779,758 | 1,509 |
| ENST00000591890.5 | hg38 | chr17 | 75,778,325 | 75,779,759 | 1,435 |
| ENST00000587560.5 | hg38 | chr17 | 75,778,567 | 75,779,286 | 720 |
| ENST00000254810.8 | hg19 | chr17 | 73,772,515 | 73,775,860 | 3,346 |
| ENST00000592643.5 | hg19 | chr17 | 73,774,331 | 73,775,839 | 1,509 |
| ENST00000591890.5 | hg19 | chr17 | 73,774,406 | 73,775,840 | 1,435 |
| ENST00000587560.5 | hg19 | chr17 | 73,774,648 | 73,775,367 | 720 |
| ENST00000589599.5 | hg19 | chr17 | 73,774,655 | 73,775,861 | 1,207 |
| ENST00000586607.5 | hg19 | chr17 | 73,774,657 | 73,781,567 | 6,911 |
| Key | Value |
|---|---|
| strand | - |
| start | 73,772,514 |
| Gene Symbol | H3F3B |
| Entrez GeneId | 3,021 |
| Chr Band | 17q25.1 |
| end | 73,776,015 |
| chr | chr17 |
| Name | H3 histone, family 3B (H3.3B) |
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