DHRS7C dehydrogenase/reductase 7C
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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42 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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 | SDR32C2 |
MIM | 616161 OMIM |
HGNC | HGNC:32423 HGNC |
Ensembl | ENSG00000184544 Ensembl |
AllianceGenome | HGNC:32423 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000330255.9 | hg38 | chr17 | 9,771,434 | 9,791,297 | 19,864 |
ENST00000571134.2 | hg38 | chr17 | 9,771,438 | 9,791,592 | 20,155 |
ENST00000330255.9 | hg19 | chr17 | 9,674,751 | 9,694,614 | 19,864 |
ENST00000571134.2 | hg19 | chr17 | 9,674,755 | 9,694,909 | 20,155 |
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