NRBP1 nuclear receptor binding protein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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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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 |
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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 | BCON3 |
SYNONYM | MADM |
SYNONYM | MUDPNP |
SYNONYM | NRBP |
MIM | 606010 OMIM |
HGNC | HGNC:7993 HGNC |
Ensembl | ENSG00000115216 Ensembl |
AllianceGenome | HGNC:7993 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000233557.7 | hg38 | chr2 | 27,427,790 | 27,442,259 | 14,470 |
ENST00000379863.7 | hg38 | chr2 | 27,428,653 | 27,442,255 | 13,603 |
ENST00000379852.8 | hg38 | chr2 | 27,428,631 | 27,442,259 | 13,629 |
ENST00000233557.7 | hg19 | chr2 | 27,650,657 | 27,665,126 | 14,470 |
ENST00000379852.8 | hg19 | chr2 | 27,651,498 | 27,665,126 | 13,629 |
ENST00000379863.7 | hg19 | chr2 | 27,651,520 | 27,665,122 | 13,603 |
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