IL1F10 interleukin 1 family member 10
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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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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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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 |
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SYNONYM | FIL1-theta |
SYNONYM | FKSG75 |
SYNONYM | IL-1HY2 |
SYNONYM | IL-38 |
SYNONYM | IL1-theta |
SYNONYM | IL1HY2 |
MIM | 615296 OMIM |
HGNC | HGNC:15552 HGNC |
Ensembl | ENSG00000136697 Ensembl |
AllianceGenome | HGNC:15552 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000393197.3 | hg38 | chr2 | 113,072,318 | 113,075,843 | 3,526 |
ENST00000341010.6 | hg38 | chr2 | 113,067,970 | 113,075,843 | 7,874 |
ENST00000341010.6 | hg19 | chr2 | 113,825,547 | 113,833,420 | 7,874 |
ENST00000393197.3 | hg19 | chr2 | 113,829,895 | 113,833,420 | 3,526 |
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