FCRLA Fc receptor like A
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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50 |
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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 |
Search Word
Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | FCRL |
SYNONYM | FCRL1 |
SYNONYM | FCRLM1 |
SYNONYM | FCRLX |
SYNONYM | FCRLb |
SYNONYM | FCRLc1 |
SYNONYM | FCRLc2 |
SYNONYM | FCRLd |
SYNONYM | FCRLe |
SYNONYM | FCRX |
SYNONYM | FREB |
MIM | 606891 OMIM |
HGNC | HGNC:18504 HGNC |
Ensembl | ENSG00000132185 Ensembl |
AllianceGenome | HGNC:18504 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000367959.6 | hg38 | chr1 | 161,706,972 | 161,714,351 | 7,380 |
ENST00000367957.7 | hg38 | chr1 | 161,707,209 | 161,714,348 | 7,140 |
ENST00000367953.7 | hg38 | chr1 | 161,707,265 | 161,714,348 | 7,084 |
ENST00000294796.8 | hg38 | chr1 | 161,707,265 | 161,713,468 | 6,204 |
ENST00000674251.1 | hg38 | chr1 | 161,706,972 | 161,714,351 | 7,380 |
ENST00000674323.1 | hg38 | chr1 | 161,706,972 | 161,714,351 | 7,380 |
ENST00000309691.10 | hg38 | chr1 | 161,707,265 | 161,713,468 | 6,204 |
ENST00000546024.5 | hg38 | chr1 | 161,706,972 | 161,714,351 | 7,380 |
ENST00000350710.3 | hg38 | chr1 | 161,706,972 | 161,714,351 | 7,380 |
ENST00000236938.12 | hg38 | chr1 | 161,707,229 | 161,714,352 | 7,124 |
ENST00000540521.5 | hg38 | chr1 | 161,706,972 | 161,714,351 | 7,380 |
ENST00000349527.8 | hg38 | chr1 | 161,707,244 | 161,713,452 | 6,209 |
ENST00000367949.6 | hg38 | chr1 | 161,706,972 | 161,714,351 | 7,380 |
ENST00000350710.3 | hg19 | chr1 | 161,676,762 | 161,684,141 | 7,380 |
ENST00000367949.6 | hg19 | chr1 | 161,676,762 | 161,684,141 | 7,380 |
ENST00000367959.6 | hg19 | chr1 | 161,676,762 | 161,684,141 | 7,380 |
ENST00000540521.5 | hg19 | chr1 | 161,676,762 | 161,684,141 | 7,380 |
ENST00000546024.5 | hg19 | chr1 | 161,676,762 | 161,684,141 | 7,380 |
ENST00000674251.1 | hg19 | chr1 | 161,676,762 | 161,684,141 | 7,380 |
ENST00000674323.1 | hg19 | chr1 | 161,676,762 | 161,684,141 | 7,380 |
ENST00000367957.7 | hg19 | chr1 | 161,676,999 | 161,684,138 | 7,140 |
ENST00000236938.12 | hg19 | chr1 | 161,677,019 | 161,684,142 | 7,124 |
ENST00000349527.8 | hg19 | chr1 | 161,677,034 | 161,683,242 | 6,209 |
ENST00000294796.8 | hg19 | chr1 | 161,677,055 | 161,683,258 | 6,204 |
ENST00000309691.10 | hg19 | chr1 | 161,677,055 | 161,683,258 | 6,204 |
ENST00000367953.7 | hg19 | chr1 | 161,677,055 | 161,684,138 | 7,084 |
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