TOLLIP toll interacting protein
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 44 |
Uncertain significance; association | 0 | 2 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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46 |
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4 |
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 |
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | IL-1RAcPIP |
MIM | 606277 OMIM |
HGNC | HGNC:16476 HGNC |
Ensembl | ENSG00000078902 Ensembl |
AllianceGenome | HGNC:16476 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000527938.5 | hg38 | chr11 | 1,277,013 | 1,309,623 | 32,611 |
ENST00000527886.5 | hg38 | chr11 | 1,274,372 | 1,302,790 | 28,419 |
ENST00000317204.11 | hg38 | chr11 | 1,274,371 | 1,309,632 | 35,262 |
ENST00000263646.11 | hg38 | chr11 | 1,275,653 | 1,309,654 | 34,002 |
ENST00000525159.5 | hg38 | chr11 | 1,274,373 | 1,309,619 | 35,247 |
ENST00000317204.11 | hg19 | chr11 | 1,295,601 | 1,330,862 | 35,262 |
ENST00000527886.5 | hg19 | chr11 | 1,295,602 | 1,324,020 | 28,419 |
ENST00000525159.5 | hg19 | chr11 | 1,295,603 | 1,330,849 | 35,247 |
ENST00000263646.11 | hg19 | chr11 | 1,296,883 | 1,330,884 | 34,002 |
ENST00000527938.5 | hg19 | chr11 | 1,298,243 | 1,330,853 | 32,611 |
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