MED29 mediator complex subunit 29
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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 |
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 | IXL |
SYNONYM | MED2 |
MIM | 612914 OMIM |
HGNC | HGNC:23074 HGNC |
Ensembl | ENSG00000063322 Ensembl |
AllianceGenome | HGNC:23074 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000615911.4 | hg38 | chr19 | 39,391,323 | 39,400,561 | 9,239 |
ENST00000315588.11 | hg38 | chr19 | 39,391,378 | 39,400,641 | 9,264 |
ENST00000594368.5 | hg38 | chr19 | 39,391,393 | 39,398,607 | 7,215 |
ENST00000615911.4 | hg19 | chr19 | 39,881,963 | 39,891,201 | 9,239 |
ENST00000315588.11 | hg19 | chr19 | 39,882,018 | 39,891,281 | 9,264 |
ENST00000594368.5 | hg19 | chr19 | 39,882,033 | 39,889,247 | 7,215 |
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