IL17RE interleukin 17 receptor E
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 78 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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90 |
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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
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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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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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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 |
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MIM | 614995 OMIM |
HGNC | HGNC:18439 HGNC |
Ensembl | ENSG00000163701 Ensembl |
AllianceGenome | HGNC:18439 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000454190.6 | hg38 | chr3 | 9,902,848 | 9,916,402 | 13,555 |
ENST00000383814.8 | hg38 | chr3 | 9,902,848 | 9,916,397 | 13,550 |
ENST00000421412.5 | hg38 | chr3 | 9,902,619 | 9,915,844 | 13,226 |
ENST00000421412.5 | hg19 | chr3 | 9,944,303 | 9,957,528 | 13,226 |
ENST00000383814.8 | hg19 | chr3 | 9,944,532 | 9,958,081 | 13,550 |
ENST00000454190.6 | hg19 | chr3 | 9,944,532 | 9,958,086 | 13,555 |
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