IL12B interleukin 12B
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 16 |
Likely pathogenic | 0 | 4 |
Benign | 0 | 30 |
Likely benign | 0 | 140 |
Conflicting classifications of pathogenicity | 0 | 16 |
Uncertain significance | 0 | 216 |
Ranking
ClinVar | |
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0 |
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0 |
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38 |
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360 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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SYNONYM | CLMF |
SYNONYM | CLMF2 |
SYNONYM | IL-12B |
SYNONYM | IMD28 |
SYNONYM | IMD29 |
SYNONYM | NKSF |
SYNONYM | NKSF2 |
MIM | 161561 OMIM |
HGNC | HGNC:5970 HGNC |
Ensembl | ENSG00000113302 Ensembl |
AllianceGenome | HGNC:5970 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000696750.1 | hg38 | chr5 | 159,314,780 | 159,330,862 | 16,083 |
ENST00000231228.3 | hg38 | chr5 | 159,314,780 | 159,330,487 | 15,708 |
ENST00000231228.3 | hg19 | chr5 | 158,741,788 | 158,757,495 | 15,708 |
ENST00000696750.1 | hg19 | chr5 | 158,741,788 | 158,757,870 | 16,083 |
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