TRIM3 tripartite motif containing 3
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 50 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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52 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | BERP |
| SYNONYM | HAC1 |
| SYNONYM | RNF22 |
| SYNONYM | RNF97 |
| MIM | 605493 OMIM |
| HGNC | HGNC:10064 HGNC |
| Ensembl | ENSG00000110171 Ensembl |
| AllianceGenome | HGNC:10064 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000359518.7 | hg38 | chr11 | 6,448,617 | 6,473,984 | 25,368 |
| ENST00000525074.5 | hg38 | chr11 | 6,448,614 | 6,474,459 | 25,846 |
| ENST00000536344.5 | hg38 | chr11 | 6,448,617 | 6,473,984 | 25,368 |
| ENST00000345851.8 | hg38 | chr11 | 6,448,613 | 6,473,941 | 25,329 |
| ENST00000345851.8 | hg19 | chr11 | 6,469,843 | 6,495,171 | 25,329 |
| ENST00000525074.5 | hg19 | chr11 | 6,469,844 | 6,495,689 | 25,846 |
| ENST00000359518.7 | hg19 | chr11 | 6,469,847 | 6,495,214 | 25,368 |
| ENST00000536344.5 | hg19 | chr11 | 6,469,847 | 6,495,214 | 25,368 |
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