RBP4 retinol binding protein 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 14 |
Likely pathogenic | 0 | 26 |
Benign | 0 | 34 |
Likely benign | 0 | 112 |
Conflicting classifications of pathogenicity | 0 | 4 |
Uncertain significance | 0 | 146 |
Ranking
ClinVar | |
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0 |
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0 |
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36 |
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292 |
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4 |
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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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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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 | MCOPCB10 |
SYNONYM | RDCCAS |
MIM | 180250 OMIM |
HGNC | HGNC:9922 HGNC |
Ensembl | ENSG00000138207 Ensembl |
AllianceGenome | HGNC:9922 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000371464.8 | hg38 | chr10 | 93,591,694 | 93,601,235 | 9,542 |
ENST00000371467.5 | hg38 | chr10 | 93,591,687 | 93,601,663 | 9,977 |
ENST00000371469.2 | hg38 | chr10 | 93,591,889 | 93,601,744 | 9,856 |
ENST00000371467.5 | hg19 | chr10 | 95,351,444 | 95,361,420 | 9,977 |
ENST00000371464.8 | hg19 | chr10 | 95,351,451 | 95,360,992 | 9,542 |
ENST00000371469.2 | hg19 | chr10 | 95,351,646 | 95,361,501 | 9,856 |
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