DLL3 delta like canonical Notch ligand 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 4 | 62 |
Likely pathogenic | 0 | 26 |
Benign | 0 | 84 |
Likely benign | 0 | 620 |
Conflicting classifications of pathogenicity | 0 | 54 |
Uncertain significance | 0 | 312 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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134 |
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922 |
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12 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
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 |
Search Word
Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | SCDO1 |
MIM | 602768 OMIM |
HGNC | HGNC:2909 HGNC |
Ensembl | ENSG00000090932 Ensembl |
AllianceGenome | HGNC:2909 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000205143.4 | hg38 | chr19 | 39,498,968 | 39,508,481 | 9,514 |
ENST00000356433.10 | hg38 | chr19 | 39,498,947 | 39,508,469 | 9,523 |
ENST00000356433.10 | hg19 | chr19 | 39,989,587 | 39,999,109 | 9,523 |
ENST00000205143.4 | hg19 | chr19 | 39,989,608 | 39,999,121 | 9,514 |
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