TRIM46 tripartite motif containing 46
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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62 |
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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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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 | GENEY |
SYNONYM | TRIFIC |
MIM | 600986 OMIM |
HGNC | HGNC:19019 HGNC |
Ensembl | ENSG00000163462 Ensembl |
AllianceGenome | HGNC:19019 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368382.5 | hg38 | chr1 | 155,173,909 | 155,184,969 | 11,061 |
ENST00000368385.8 | hg38 | chr1 | 155,173,878 | 155,180,621 | 6,744 |
ENST00000368383.7 | hg38 | chr1 | 155,173,900 | 155,182,862 | 8,963 |
ENST00000543729.5 | hg38 | chr1 | 155,173,891 | 155,179,935 | 6,045 |
ENST00000334634.9 | hg38 | chr1 | 155,173,849 | 155,184,970 | 11,122 |
ENST00000545012.5 | hg38 | chr1 | 155,173,787 | 155,184,971 | 11,185 |
ENST00000611379.1 | hg38 | chr1 | 155,174,754 | 155,184,971 | 10,218 |
ENST00000545012.5 | hg19 | chr1 | 155,146,263 | 155,157,447 | 11,185 |
ENST00000334634.9 | hg19 | chr1 | 155,146,325 | 155,157,446 | 11,122 |
ENST00000368385.8 | hg19 | chr1 | 155,146,354 | 155,153,097 | 6,744 |
ENST00000543729.5 | hg19 | chr1 | 155,146,367 | 155,152,411 | 6,045 |
ENST00000368383.7 | hg19 | chr1 | 155,146,376 | 155,155,338 | 8,963 |
ENST00000368382.5 | hg19 | chr1 | 155,146,385 | 155,157,445 | 11,061 |
ENST00000611379.1 | hg19 | chr1 | 155,147,230 | 155,157,447 | 10,218 |
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