SDC1 syndecan 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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2 |
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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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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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 | CD138 |
SYNONYM | SDC |
SYNONYM | SYND1 |
SYNONYM | syndecan |
MIM | 186355 OMIM |
HGNC | HGNC:10658 HGNC |
Ensembl | ENSG00000115884 Ensembl |
AllianceGenome | HGNC:10658 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000254351.9 | hg38 | chr2 | 20,200,797 | 20,225,130 | 24,334 |
ENST00000381150.5 | hg38 | chr2 | 20,200,799 | 20,225,433 | 24,635 |
ENST00000403076.5 | hg38 | chr2 | 20,201,486 | 20,225,096 | 23,611 |
ENST00000254351.9 | hg19 | chr2 | 20,400,558 | 20,424,891 | 24,334 |
ENST00000381150.5 | hg19 | chr2 | 20,400,560 | 20,425,194 | 24,635 |
ENST00000403076.5 | hg19 | chr2 | 20,401,247 | 20,424,857 | 23,611 |
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