SPARCL1 SPARC like 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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64 |
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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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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 | MAST 9 |
SYNONYM | MAST9 |
SYNONYM | PIG33 |
SYNONYM | SC1 |
MIM | 606041 OMIM |
HGNC | HGNC:11220 HGNC |
Ensembl | ENSG00000152583 Ensembl |
AllianceGenome | HGNC:11220 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000282470.11 | hg38 | chr4 | 87,473,335 | 87,529,376 | 56,042 |
ENST00000503414.5 | hg38 | chr4 | 87,473,418 | 87,529,092 | 55,675 |
ENST00000418378.5 | hg38 | chr4 | 87,473,348 | 87,529,503 | 56,156 |
ENST00000282470.11 | hg19 | chr4 | 88,394,487 | 88,450,528 | 56,042 |
ENST00000418378.5 | hg19 | chr4 | 88,394,500 | 88,450,655 | 56,156 |
ENST00000503414.5 | hg19 | chr4 | 88,394,570 | 88,450,244 | 55,675 |
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