TRIM16 tripartite motif containing 16
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 12 |
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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64 |
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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 | EBBP |
MIM | 609505 OMIM |
HGNC | HGNC:17241 HGNC |
Ensembl | ENSG00000221926 Ensembl |
AllianceGenome | HGNC:17241 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000577886.5 | hg38 | chr17 | 15,627,960 | 15,642,964 | 15,005 |
ENST00000649191.2 | hg38 | chr17 | 15,627,966 | 15,684,311 | 56,346 |
ENST00000579219.5 | hg38 | chr17 | 15,628,648 | 15,642,934 | 14,287 |
ENST00000578237.5 | hg38 | chr17 | 15,627,960 | 15,684,300 | 56,341 |
ENST00000336708.11 | hg38 | chr17 | 15,627,967 | 15,682,879 | 54,913 |
ENST00000416464.6 | hg38 | chr17 | 15,627,960 | 15,684,299 | 56,340 |
ENST00000416464.6 | hg19 | chr17 | 15,531,274 | 15,587,613 | 56,340 |
ENST00000336708.11 | hg19 | chr17 | 15,531,281 | 15,586,193 | 54,913 |
ENST00000577886.5 | hg19 | chr17 | 15,531,274 | 15,546,278 | 15,005 |
ENST00000578237.5 | hg19 | chr17 | 15,531,274 | 15,587,614 | 56,341 |
ENST00000579219.5 | hg19 | chr17 | 15,531,962 | 15,546,248 | 14,287 |
ENST00000649191.2 | hg19 | chr17 | 15,531,280 | 15,587,625 | 56,346 |
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