DCST1 DC-STAMP domain containing 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 88 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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100 |
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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
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 | SNKY |
SYNONYM | SPE49 |
MIM | 619860 OMIM |
HGNC | HGNC:26539 HGNC |
Ensembl | ENSG00000163357 Ensembl |
AllianceGenome | HGNC:26539 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000423025.6 | hg38 | chr1 | 155,033,829 | 155,050,930 | 17,102 |
ENST00000368419.2 | hg38 | chr1 | 155,033,970 | 155,049,264 | 15,295 |
ENST00000295542.6 | hg38 | chr1 | 155,033,824 | 155,050,930 | 17,107 |
ENST00000295542.6 | hg19 | chr1 | 155,006,300 | 155,023,406 | 17,107 |
ENST00000423025.6 | hg19 | chr1 | 155,006,305 | 155,023,406 | 17,102 |
ENST00000368419.2 | hg19 | chr1 | 155,006,446 | 155,021,740 | 15,295 |
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