MINK1 misshapen like kinase 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 20 |
Likely benign | 0 | 18 |
Uncertain significance | 0 | 136 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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174 |
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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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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 | B55 |
SYNONYM | MAP4K6 |
SYNONYM | MEKKK 6 |
SYNONYM | MINK |
SYNONYM | YSK2 |
SYNONYM | ZC3 |
MIM | 609426 OMIM |
HGNC | HGNC:17565 HGNC |
Ensembl | ENSG00000141503 Ensembl |
AllianceGenome | HGNC:17565 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000347992.11 | hg38 | chr17 | 4,833,400 | 4,898,054 | 64,655 |
ENST00000355280.11 | hg38 | chr17 | 4,833,340 | 4,898,061 | 64,722 |
ENST00000453408.7 | hg38 | chr17 | 4,833,584 | 4,897,287 | 63,704 |
ENST00000355280.11 | hg19 | chr17 | 4,736,635 | 4,801,356 | 64,722 |
ENST00000347992.11 | hg19 | chr17 | 4,736,695 | 4,801,349 | 64,655 |
ENST00000453408.7 | hg19 | chr17 | 4,736,879 | 4,800,582 | 63,704 |
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