CEP76 centrosomal protein 76
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 6 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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60 |
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6 |
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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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 | C18orf9 |
SYNONYM | HsT1705 |
MIM | 620791 OMIM |
HGNC | HGNC:25727 HGNC |
Ensembl | ENSG00000101624 Ensembl |
AllianceGenome | HGNC:25727 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000262127.7 | hg38 | chr18 | 12,672,625 | 12,702,723 | 30,099 |
ENST00000423709.6 | hg38 | chr18 | 12,673,097 | 12,702,722 | 29,626 |
ENST00000262127.7 | hg19 | chr18 | 12,672,624 | 12,702,722 | 30,099 |
ENST00000423709.6 | hg19 | chr18 | 12,673,096 | 12,702,721 | 29,626 |
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