HSF2 heat shock transcription factor 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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32 |
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2 |
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
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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 |
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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 | HSF 2 |
SYNONYM | HSTF 2 |
MIM | 140581 OMIM |
HGNC | HGNC:5225 HGNC |
Ensembl | ENSG00000025156 Ensembl |
AllianceGenome | HGNC:5225 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000452194.5 | hg38 | chr6 | 122,399,551 | 122,433,119 | 33,569 |
ENST00000368455.9 | hg38 | chr6 | 122,399,652 | 122,433,119 | 33,468 |
ENST00000452194.5 | hg19 | chr6 | 122,720,696 | 122,754,264 | 33,569 |
ENST00000368455.9 | hg19 | chr6 | 122,720,797 | 122,754,264 | 33,468 |
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