DHRS7B dehydrogenase/reductase 7B
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | CGI-93 |
SYNONYM | SDR32C1 |
MIM | 616160 OMIM |
HGNC | HGNC:24547 HGNC |
Ensembl | ENSG00000109016 Ensembl |
AllianceGenome | HGNC:24547 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000581463.1 | hg38 | chr17 | 21,184,385 | 21,193,265 | 8,881 |
ENST00000395511.8 | hg38 | chr17 | 21,126,964 | 21,191,420 | 64,457 |
ENST00000579303.5 | hg38 | chr17 | 21,126,964 | 21,191,445 | 64,482 |
ENST00000395511.8 | hg19 | chr17 | 21,030,277 | 21,094,733 | 64,457 |
ENST00000579303.5 | hg19 | chr17 | 21,030,277 | 21,094,758 | 64,482 |
ENST00000581463.1 | hg19 | chr17 | 21,087,698 | 21,096,578 | 8,881 |
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