FCRL6 Fc receptor like 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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76 |
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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 | FcRH6 |
MIM | 613562 OMIM |
HGNC | HGNC:31910 HGNC |
Ensembl | ENSG00000181036 Ensembl |
AllianceGenome | HGNC:31910 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000321935.10 | hg38 | chr1 | 159,800,512 | 159,816,251 | 15,740 |
ENST00000368106.4 | hg38 | chr1 | 159,802,360 | 159,816,257 | 13,898 |
ENST00000339348.9 | hg38 | chr1 | 159,802,417 | 159,815,802 | 13,386 |
ENST00000392235.7 | hg38 | chr1 | 159,802,424 | 159,815,592 | 13,169 |
ENST00000321935.10 | hg19 | chr1 | 159,770,302 | 159,786,041 | 15,740 |
ENST00000368106.4 | hg19 | chr1 | 159,772,150 | 159,786,047 | 13,898 |
ENST00000339348.9 | hg19 | chr1 | 159,772,207 | 159,785,592 | 13,386 |
ENST00000392235.7 | hg19 | chr1 | 159,772,214 | 159,785,382 | 13,169 |
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