TRIM34 tripartite motif containing 34
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 2 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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0 |
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2 |
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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Search word | : | |
Filtering | : |
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 | IFP1 |
SYNONYM | RNF21 |
MIM | 605684 OMIM |
HGNC | HGNC:10063 HGNC |
Ensembl | ENSG00000258659 Ensembl |
AllianceGenome | HGNC:10063 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000514226.5 | hg38 | chr11 | 5,619,764 | 5,644,398 | 24,635 |
ENST00000429814.3 | hg38 | chr11 | 5,625,001 | 5,644,398 | 19,398 |
ENST00000514226.5 | hg19 | chr11 | 5,640,994 | 5,665,628 | 24,635 |
ENST00000429814.3 | hg19 | chr11 | 5,646,231 | 5,665,628 | 19,398 |
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