CETN3 centrin 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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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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 | CDC31 |
SYNONYM | CEN3 |
MIM | 602907 OMIM |
HGNC | HGNC:1868 HGNC |
Ensembl | ENSG00000153140 Ensembl |
AllianceGenome | HGNC:1868 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000522565.5 | hg38 | chr5 | 90,399,047 | 90,409,757 | 10,711 |
ENST00000283122.8 | hg38 | chr5 | 90,392,257 | 90,409,756 | 17,500 |
ENST00000522842.1 | hg38 | chr5 | 90,405,394 | 90,409,766 | 4,373 |
ENST00000522864.5 | hg38 | chr5 | 90,393,859 | 90,409,732 | 15,874 |
ENST00000522083.5 | hg38 | chr5 | 90,393,710 | 90,409,757 | 16,048 |
ENST00000283122.8 | hg19 | chr5 | 89,688,074 | 89,705,573 | 17,500 |
ENST00000522083.5 | hg19 | chr5 | 89,689,527 | 89,705,574 | 16,048 |
ENST00000522864.5 | hg19 | chr5 | 89,689,676 | 89,705,549 | 15,874 |
ENST00000522565.5 | hg19 | chr5 | 89,694,864 | 89,705,574 | 10,711 |
ENST00000522842.1 | hg19 | chr5 | 89,701,211 | 89,705,583 | 4,373 |
Key | Value |
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strand | - |
start | 89,689,151 |
Gene Symbol | CETN3 |
Entrez GeneId | 1,070 |
Chr Band | 5q14.3 |
end | 89,705,602 |
chr | chr5 |
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