IL18BP interleukin 18 binding protein
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 16 |
Likely benign | 0 | 34 |
Conflicting classifications of pathogenicity | 0 | 2 |
risk factor | 0 | 2 |
Uncertain significance | 0 | 234 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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14 |
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270 |
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2 |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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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SYNONYM | FVH |
SYNONYM | IL18BPa |
MIM | 604113 OMIM |
HGNC | HGNC:5987 HGNC |
Ensembl | ENSG00000137496 Ensembl |
AllianceGenome | HGNC:5987 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000698841.1 | hg38 | chr11 | 71,999,926 | 72,001,944 | 2,019 |
ENST00000620017.4 | hg38 | chr11 | 71,998,912 | 72,002,804 | 3,893 |
ENST00000497194.6 | hg38 | chr11 | 71,998,613 | 72,003,753 | 5,141 |
ENST00000393707.4 | hg38 | chr11 | 71,999,927 | 72,002,527 | 2,601 |
ENST00000393705.8 | hg38 | chr11 | 71,998,892 | 72,002,527 | 3,636 |
ENST00000393703.9 | hg38 | chr11 | 71,998,909 | 72,002,804 | 3,896 |
ENST00000337131.9 | hg38 | chr11 | 71,998,912 | 72,002,527 | 3,616 |
ENST00000404792.5 | hg38 | chr11 | 71,999,063 | 72,002,526 | 3,464 |
ENST00000531053.5 | hg38 | chr11 | 71,998,925 | 72,001,745 | 2,821 |
ENST00000393705.8 | hg19 | chr11 | 71,709,938 | 71,713,573 | 3,636 |
ENST00000393707.4 | hg19 | chr11 | 71,710,973 | 71,713,573 | 2,601 |
ENST00000497194.6 | hg19 | chr11 | 71,709,659 | 71,714,799 | 5,141 |
ENST00000393703.9 | hg19 | chr11 | 71,709,955 | 71,713,850 | 3,896 |
ENST00000337131.9 | hg19 | chr11 | 71,709,958 | 71,713,573 | 3,616 |
ENST00000404792.5 | hg19 | chr11 | 71,710,109 | 71,713,572 | 3,464 |
ENST00000531053.5 | hg19 | chr11 | 71,709,971 | 71,712,791 | 2,821 |
ENST00000620017.4 | hg19 | chr11 | 71,709,958 | 71,713,850 | 3,893 |
ENST00000698841.1 | hg19 | chr11 | 71,710,972 | 71,712,990 | 2,019 |
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