FCGR2A Fc gamma receptor IIa
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 16 |
| Likely benign | 0 | 20 |
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
6 |
 |
60 |
 |
4 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CD32 |
| SYNONYM | CD32A |
| SYNONYM | CDw32 |
| SYNONYM | FCG2 |
| SYNONYM | FCGR2 |
| SYNONYM | FCGR2A1 |
| SYNONYM | FcGR |
| SYNONYM | FcgammaRIIa |
| SYNONYM | IGFR2 |
| MIM | 146790 OMIM |
| HGNC | HGNC:3616 HGNC |
| Ensembl | ENSG00000143226 Ensembl |
| AllianceGenome | HGNC:3616 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000271450.12 | hg38 | chr1 | 161,505,457 | 161,519,829 | 14,373 |
| ENST00000367972.8 | hg38 | chr1 | 161,505,430 | 161,518,558 | 13,129 |
| ENST00000699277.1 | hg38 | chr1 | 161,505,456 | 161,519,553 | 14,098 |
| ENST00000699278.1 | hg38 | chr1 | 161,505,457 | 161,519,554 | 14,098 |
| ENST00000699279.1 | hg38 | chr1 | 161,505,869 | 161,519,554 | 13,686 |
| ENST00000367972.8 | hg19 | chr1 | 161,475,220 | 161,488,348 | 13,129 |
| ENST00000271450.12 | hg19 | chr1 | 161,475,247 | 161,489,619 | 14,373 |
| ENST00000699277.1 | hg19 | chr1 | 161,475,246 | 161,489,343 | 14,098 |
| ENST00000699278.1 | hg19 | chr1 | 161,475,247 | 161,489,344 | 14,098 |
| ENST00000699279.1 | hg19 | chr1 | 161,475,659 | 161,489,344 | 13,686 |
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