CEACAM7 CEA cell adhesion molecule 7
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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30 |
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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
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 |
Search Word
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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Category | : |
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Search word | : | |
Filtering | : |
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 | CGM2 |
MIM | 619160 OMIM |
HGNC | HGNC:1819 HGNC |
Ensembl | ENSG00000007306 Ensembl |
AllianceGenome | HGNC:1819 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000006724.7 | hg38 | chr19 | 41,673,307 | 41,688,367 | 15,061 |
ENST00000401731.6 | hg38 | chr19 | 41,673,303 | 41,688,270 | 14,968 |
ENST00000602225.1 | hg38 | chr19 | 41,677,409 | 41,688,167 | 10,759 |
ENST00000401731.6 | hg19 | chr19 | 42,177,231 | 42,192,199 | 14,969 |
ENST00000006724.7 | hg19 | chr19 | 42,177,235 | 42,192,296 | 15,062 |
ENST00000602225.1 | hg19 | chr19 | 42,181,337 | 42,192,096 | 10,760 |
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