HOXA10 homeobox A10
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 10 |
| Likely benign | 0 | 14 |
| Uncertain significance | 0 | 60 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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2 |
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80 |
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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
[No Data.]
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
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| 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 | HOX1 |
| SYNONYM | HOX1.8 |
| SYNONYM | HOX1H |
| SYNONYM | PL |
| MIM | 142957 OMIM |
| HGNC | HGNC:5100 HGNC |
| Ensembl | ENSG00000253293 Ensembl |
| AllianceGenome | HGNC:5100 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000396344.4 | hg38 | chr7 | 27,171,220 | 27,180,261 | 9,042 |
| ENST00000283921.5 | hg38 | chr7 | 27,170,605 | 27,174,320 | 3,716 |
| ENST00000283921.5 | hg19 | chr7 | 27,210,224 | 27,213,939 | 3,716 |
| ENST00000396344.4 | hg19 | chr7 | 27,210,839 | 27,219,880 | 9,042 |
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