FCER1A Fc epsilon receptor Ia
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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44 |
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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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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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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 | FCE1A |
SYNONYM | FCERIA |
SYNONYM | FcERI |
MIM | 147140 OMIM |
HGNC | HGNC:3609 HGNC |
Ensembl | ENSG00000179639 Ensembl |
AllianceGenome | HGNC:3609 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368115.5 | hg38 | chr1 | 159,289,714 | 159,308,224 | 18,511 |
ENST00000368114.1 | hg38 | chr1 | 159,302,336 | 159,307,993 | 5,658 |
ENST00000693622.1 | hg38 | chr1 | 159,302,336 | 159,308,202 | 5,867 |
ENST00000368115.5 | hg19 | chr1 | 159,259,504 | 159,278,014 | 18,511 |
ENST00000368114.1 | hg19 | chr1 | 159,272,126 | 159,277,783 | 5,658 |
ENST00000693622.1 | hg19 | chr1 | 159,272,126 | 159,277,992 | 5,867 |
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