MAPKAPK2 MAPK activated protein kinase 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
not provided | 3 | 0 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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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
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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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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 | MAPKAP-K2 |
SYNONYM | MK-2 |
SYNONYM | MK2 |
MIM | 602006 OMIM |
HGNC | HGNC:6887 HGNC |
Ensembl | ENSG00000162889 Ensembl |
AllianceGenome | HGNC:6887 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000294981.8 | hg38 | chr1 | 206,684,944 | 206,732,863 | 47,920 |
ENST00000367103.4 | hg38 | chr1 | 206,684,905 | 206,734,281 | 49,377 |
ENST00000367103.4 | hg19 | chr1 | 206,858,250 | 206,907,626 | 49,377 |
ENST00000294981.8 | hg19 | chr1 | 206,858,289 | 206,906,208 | 47,920 |
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