TMEM114 transmembrane protein 114
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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 |
Search Word
Target data | : |
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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MIM | 611579 OMIM |
HGNC | HGNC:33227 HGNC |
Ensembl | ENSG00000232258 Ensembl |
AllianceGenome | HGNC:33227 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000620492.5 | hg38 | chr16 | 8,569,500 | 8,590,511 | 21,012 |
ENST00000568335.3 | hg38 | chr16 | 8,569,500 | 8,590,193 | 20,694 |
ENST00000624696.1 | hg38 | chr16 | 8,569,747 | 8,589,838 | 20,092 |
ENST00000568335.3 | hg19 | chr16 | 8,619,502 | 8,622,226 | 2,725 |
ENST00000620492.5 | hg19 | chr16 | 8,619,502 | 8,622,226 | 2,725 |
ENST00000624696.1 | hg19 | chr16 | 8,619,749 | 8,620,007 | 259 |
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