NRK Nik related kinase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 26 |
not provided | 6 | 0 |
Uncertain significance | 0 | 114 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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150 |
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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
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 | NESK |
MIM | 300791 OMIM |
HGNC | HGNC:25391 HGNC |
Ensembl | ENSG00000123572 Ensembl |
AllianceGenome | HGNC:25391 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000540278.1 | hg38 | chrX | 105,948,438 | 105,956,593 | 8,156 |
ENST00000536164.5 | hg38 | chrX | 105,822,553 | 105,895,363 | 72,811 |
ENST00000243300.14 | hg38 | chrX | 105,822,539 | 105,958,610 | 136,072 |
ENST00000243300.14 | hg19 | chrX | 105,066,532 | 105,202,602 | 136,071 |
ENST00000536164.5 | hg19 | chrX | 105,066,546 | 105,139,356 | 72,811 |
ENST00000540278.1 | hg19 | chrX | 105,192,430 | 105,200,585 | 8,156 |
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