CDCA3 cell division cycle associated 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 24 |
Likely benign | 0 | 50 |
Uncertain significance | 0 | 120 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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16 |
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178 |
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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
[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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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 | GRCC8 |
SYNONYM | TOME-1 |
SYNONYM | TOME1 |
MIM | 607749 OMIM |
HGNC | HGNC:14624 HGNC |
Ensembl | ENSG00000111665 Ensembl |
AllianceGenome | HGNC:14624 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000422785.7 | hg38 | chr12 | 6,844,793 | 6,851,269 | 6,477 |
ENST00000535406.5 | hg38 | chr12 | 6,848,829 | 6,851,258 | 2,430 |
ENST00000538862.7 | hg38 | chr12 | 6,848,828 | 6,851,286 | 2,459 |
ENST00000229265.10 | hg38 | chr12 | 6,848,816 | 6,851,252 | 2,437 |
ENST00000540683.1 | hg38 | chr12 | 6,848,843 | 6,851,249 | 2,407 |
ENST00000422785.7 | hg19 | chr12 | 6,953,957 | 6,960,433 | 6,477 |
ENST00000229265.10 | hg19 | chr12 | 6,957,980 | 6,960,416 | 2,437 |
ENST00000538862.7 | hg19 | chr12 | 6,957,992 | 6,960,450 | 2,459 |
ENST00000535406.5 | hg19 | chr12 | 6,957,993 | 6,960,422 | 2,430 |
ENST00000540683.1 | hg19 | chr12 | 6,958,007 | 6,960,413 | 2,407 |
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