ASGR2 asialoglycoprotein receptor 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 36 |
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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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 |
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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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | ASGP-R2 |
SYNONYM | ASGPR2 |
SYNONYM | CLEC4H2 |
SYNONYM | HBXBP |
SYNONYM | HL-2 |
MIM | 108361 OMIM |
HGNC | HGNC:743 HGNC |
Ensembl | ENSG00000161944 Ensembl |
AllianceGenome | HGNC:743 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000254850.11 | hg38 | chr17 | 7,101,322 | 7,114,823 | 13,502 |
ENST00000355035.9 | hg38 | chr17 | 7,101,322 | 7,114,653 | 13,332 |
ENST00000446679.6 | hg38 | chr17 | 7,101,575 | 7,114,240 | 12,666 |
ENST00000691900.1 | hg38 | chr17 | 7,101,326 | 7,114,822 | 13,497 |
ENST00000355035.9 | hg19 | chr17 | 7,004,641 | 7,017,972 | 13,332 |
ENST00000254850.11 | hg19 | chr17 | 7,004,641 | 7,018,142 | 13,502 |
ENST00000691900.1 | hg19 | chr17 | 7,004,645 | 7,018,141 | 13,497 |
ENST00000446679.6 | hg19 | chr17 | 7,004,894 | 7,017,559 | 12,666 |
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