COLCA1 colorectal cancer associated 1
Information
Clinical Significance
MGeND | ClinVar |
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Ranking
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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
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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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 | C11orf92 |
SYNONYM | CASC12 |
SYNONYM | LOH11CR1F |
MIM | 615693 OMIM |
HGNC | HGNC:33789 HGNC |
Ensembl | ENSG00000196167 Ensembl |
AllianceGenome | HGNC:33789 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000620864.1 | hg38 | chr11 | 111,290,787 | 111,305,045 | 14,259 |
ENST00000620864.1 | hg19 | chr11 | 111,161,512 | 111,175,770 | 14,259 |
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