ICAM1 intercellular adhesion molecule 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 20 |
Likely benign | 0 | 26 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
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0 |
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0 |
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10 |
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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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SYNONYM | BB2 |
SYNONYM | CD54 |
SYNONYM | P3.58 |
MIM | 147840 OMIM |
HGNC | HGNC:5344 HGNC |
Ensembl | ENSG00000090339 Ensembl |
AllianceGenome | HGNC:5344 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000423829.2 | hg38 | chr19 | 10,271,093 | 10,285,583 | 14,491 |
ENST00000264832.8 | hg38 | chr19 | 10,271,120 | 10,286,615 | 15,496 |
ENST00000423829.2 | hg19 | chr19 | 10,381,769 | 10,396,259 | 14,491 |
ENST00000264832.8 | hg19 | chr19 | 10,381,796 | 10,397,291 | 15,496 |
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