H3-7 H3.7 histone (putative)
Information
- Symbol
- H3-7
- Type
- protein-coding
- Description
- H3.7 histone (putative)
- Entrez Gene ID
- 440686
- Genome
- hg19
- Position
- chr1:149,396,963-149,400,542
- Genome
- hg38
- Position
- chr1:143,902,387-143,905,966
- HGNC
- HGNC:32060 HGNC
- Ensembl
- ENSG00000273213 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 1 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
4 |
 |
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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| Category | : |
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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 | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
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| Search word | : | |
| Filtering | : |
| 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 | H3-2 |
| SYNONYM | H3.7 |
| SYNONYM | HIST2H3PS2 |
| SYNONYM | p06 |
| HGNC | HGNC:32060 HGNC |
| Ensembl | ENSG00000273213 Ensembl |
| AllianceGenome | HGNC:32060 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000609879.2 | hg38 | chr1 | 143,902,387 | 143,905,966 | 3,580 |
| ENST00000392948.5 | hg38 | chr1 | 143,905,510 | 143,905,977 | 468 |
| ENST00000609879.2 | hg19 | chr1 | 149,396,963 | 149,400,542 | 3,580 |
| ENST00000392948.5 | hg19 | chr1 | 149,400,086 | 149,400,553 | 468 |
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