DECR2 2,4-dienoyl-CoA reductase 2
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 80 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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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
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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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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 | PDCR |
SYNONYM | SDR17C1 |
MIM | 615839 OMIM |
HGNC | HGNC:2754 HGNC |
Ensembl | ENSG00000242612 Ensembl |
AllianceGenome | HGNC:2754 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000627716.2 | hg38 | chr16 | 401,858 | 406,729 | 4,872 |
ENST00000219481.10 | hg38 | chr16 | 401,885 | 412,482 | 10,598 |
ENST00000424398.6 | hg38 | chr16 | 401,882 | 411,976 | 10,095 |
ENST00000424398.6 | hg19 | chr16 | 451,882 | 461,976 | 10,095 |
ENST00000627716.2 | hg19 | chr16 | 451,858 | 456,729 | 4,872 |
ENST00000219481.10 | hg19 | chr16 | 451,885 | 462,482 | 10,598 |
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