RDH5 retinol dehydrogenase 5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 24 | 74 |
Likely pathogenic | 0 | 18 |
Benign | 0 | 30 |
Likely benign | 0 | 144 |
Conflicting classifications of pathogenicity | 0 | 16 |
Uncertain significance | 0 | 262 |
Ranking
ClinVar | |
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0 |
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0 |
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64 |
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438 |
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10 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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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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 | 9cRDH |
SYNONYM | HSD17B9 |
SYNONYM | RDH1 |
SYNONYM | SDR9C5 |
MIM | 601617 OMIM |
HGNC | HGNC:9940 HGNC |
Ensembl | ENSG00000135437 Ensembl |
AllianceGenome | HGNC:9940 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000547072.5 | hg38 | chr12 | 55,720,367 | 55,724,606 | 4,240 |
ENST00000257895.10 | hg38 | chr12 | 55,720,393 | 55,724,705 | 4,313 |
ENST00000548082.1 | hg38 | chr12 | 55,720,413 | 55,724,705 | 4,293 |
ENST00000547072.5 | hg19 | chr12 | 56,114,151 | 56,118,390 | 4,240 |
ENST00000257895.10 | hg19 | chr12 | 56,114,177 | 56,118,489 | 4,313 |
ENST00000548082.1 | hg19 | chr12 | 56,114,197 | 56,118,489 | 4,293 |
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