TRIM6 tripartite motif containing 6
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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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Category | : |
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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 |
---|---|
SYNONYM | RNF89 |
MIM | 607564 OMIM |
HGNC | HGNC:16277 HGNC |
Ensembl | ENSG00000121236 Ensembl |
AllianceGenome | HGNC:16277 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000445329.5 | hg38 | chr11 | 5,596,746 | 5,612,952 | 16,207 |
ENST00000621176.1 | hg38 | chr11 | 5,603,313 | 5,612,958 | 9,646 |
ENST00000380097.8 | hg38 | chr11 | 5,596,637 | 5,612,952 | 16,316 |
ENST00000515022.5 | hg38 | chr11 | 5,596,806 | 5,611,345 | 14,540 |
ENST00000506134.5 | hg38 | chr11 | 5,596,806 | 5,611,587 | 14,782 |
ENST00000278302.9 | hg38 | chr11 | 5,596,109 | 5,612,952 | 16,844 |
ENST00000380107.5 | hg38 | chr11 | 5,596,129 | 5,612,423 | 16,295 |
ENST00000507320.5 | hg38 | chr11 | 5,596,113 | 5,611,700 | 15,588 |
ENST00000278302.9 | hg19 | chr11 | 5,617,339 | 5,634,182 | 16,844 |
ENST00000507320.5 | hg19 | chr11 | 5,617,343 | 5,632,930 | 15,588 |
ENST00000380107.5 | hg19 | chr11 | 5,617,359 | 5,633,653 | 16,295 |
ENST00000380097.8 | hg19 | chr11 | 5,617,867 | 5,634,182 | 16,316 |
ENST00000445329.5 | hg19 | chr11 | 5,617,976 | 5,634,182 | 16,207 |
ENST00000515022.5 | hg19 | chr11 | 5,618,036 | 5,632,575 | 14,540 |
ENST00000506134.5 | hg19 | chr11 | 5,618,036 | 5,632,817 | 14,782 |
ENST00000621176.1 | hg19 | chr11 | 5,624,543 | 5,634,188 | 9,646 |
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