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 |
![]() |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | SCDO1 |
| MIM | 602768 OMIM |
| HGNC | HGNC:2909 HGNC |
| Ensembl | ENSG00000090932 Ensembl |
| AllianceGenome | HGNC:2909 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| 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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