NRIP3 nuclear receptor interacting protein 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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
Search Word
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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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 | C11orf14 |
SYNONYM | NY-SAR-105 |
MIM | 613125 OMIM |
HGNC | HGNC:1167 HGNC |
Ensembl | ENSG00000175352 Ensembl |
AllianceGenome | HGNC:1167 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000309166.8 | hg38 | chr11 | 8,980,576 | 9,004,001 | 23,426 |
ENST00000696747.1 | hg38 | chr11 | 8,965,682 | 9,004,651 | 38,970 |
ENST00000531090.5 | hg38 | chr11 | 8,983,579 | 9,004,049 | 20,471 |
ENST00000696747.1 | hg19 | chr11 | 8,987,229 | 9,026,198 | 38,970 |
ENST00000309166.8 | hg19 | chr11 | 9,002,123 | 9,025,548 | 23,426 |
ENST00000531090.5 | hg19 | chr11 | 9,005,126 | 9,025,596 | 20,471 |
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