LGALS9 galectin 9
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
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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66 |
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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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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 | HUAT |
SYNONYM | LGALS9A |
MIM | 601879 OMIM |
HGNC | HGNC:6570 HGNC |
Ensembl | ENSG00000168961 Ensembl |
AllianceGenome | HGNC:6570 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000313648.10 | hg38 | chr17 | 27,631,148 | 27,649,433 | 18,286 |
ENST00000302228.9 | hg38 | chr17 | 27,629,798 | 27,649,560 | 19,763 |
ENST00000395473.7 | hg38 | chr17 | 27,631,188 | 27,649,560 | 18,373 |
ENST00000302228.9 | hg19 | chr17 | 25,956,824 | 25,976,586 | 19,763 |
ENST00000313648.10 | hg19 | chr17 | 25,958,174 | 25,976,459 | 18,286 |
ENST00000395473.7 | hg19 | chr17 | 25,958,214 | 25,976,586 | 18,373 |
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