MED21 mediator complex subunit 21
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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4 |
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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
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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 |
Search Word
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 | SRB7 |
SYNONYM | SURB7 |
SYNONYM | hSrb7 |
MIM | 603800 OMIM |
HGNC | HGNC:11473 HGNC |
Ensembl | ENSG00000152944 Ensembl |
AllianceGenome | HGNC:11473 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000282892.4 | hg38 | chr12 | 27,022,558 | 27,030,673 | 8,116 |
ENST00000546323.5 | hg38 | chr12 | 27,022,546 | 27,030,756 | 8,211 |
ENST00000546323.5 | hg19 | chr12 | 27,175,479 | 27,183,689 | 8,211 |
ENST00000282892.4 | hg19 | chr12 | 27,175,491 | 27,183,606 | 8,116 |
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