SKIC8 SKI8 subunit of superkiller complex
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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10 |
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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 |
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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 | REC14 |
SYNONYM | SKI8 |
SYNONYM | WDR61 |
MIM | 609540 OMIM |
HGNC | HGNC:30300 HGNC |
Ensembl | ENSG00000140395 Ensembl |
AllianceGenome | HGNC:30300 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000558459.5 | hg38 | chr15 | 78,283,256 | 78,299,591 | 16,336 |
ENST00000558311.5 | hg38 | chr15 | 78,283,235 | 78,299,605 | 16,371 |
ENST00000267973.7 | hg38 | chr15 | 78,283,235 | 78,299,609 | 16,375 |
ENST00000558311.5 | hg19 | chr15 | 78,575,577 | 78,591,947 | 16,371 |
ENST00000267973.7 | hg19 | chr15 | 78,575,577 | 78,591,951 | 16,375 |
ENST00000558459.5 | hg19 | chr15 | 78,575,598 | 78,591,933 | 16,336 |
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