CDC6 cell division cycle 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 24 |
Likely benign | 0 | 108 |
Conflicting classifications of pathogenicity | 0 | 18 |
not provided | 2 | 0 |
Uncertain significance | 0 | 214 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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36 |
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308 |
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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
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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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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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 |
---|---|
SYNONYM | CDC18L |
SYNONYM | HsCDC18 |
SYNONYM | HsCDC6 |
SYNONYM | MGORS5 |
MIM | 602627 OMIM |
HGNC | HGNC:1744 HGNC |
Ensembl | ENSG00000094804 Ensembl |
AllianceGenome | HGNC:1744 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000209728.9 | hg38 | chr17 | 40,287,879 | 40,304,657 | 16,779 |
ENST00000649662.1 | hg38 | chr17 | 40,287,933 | 40,302,236 | 14,304 |
ENST00000209728.9 | hg19 | chr17 | 38,444,131 | 38,460,909 | 16,779 |
ENST00000649662.1 | hg19 | chr17 | 38,444,185 | 38,458,488 | 14,304 |
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