CD68 CD68 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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56 |
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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 | GP110 |
SYNONYM | LAMP4 |
SYNONYM | SCARD1 |
MIM | 153634 OMIM |
HGNC | HGNC:1693 HGNC |
Ensembl | ENSG00000129226 Ensembl |
AllianceGenome | HGNC:1693 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000250092.11 | hg38 | chr17 | 7,579,638 | 7,582,111 | 2,474 |
ENST00000380498.10 | hg38 | chr17 | 7,579,491 | 7,582,111 | 2,621 |
ENST00000380498.10 | hg19 | chr17 | 7,482,809 | 7,485,429 | 2,621 |
ENST00000250092.11 | hg19 | chr17 | 7,482,956 | 7,485,429 | 2,474 |
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