CEACAM5 CEA cell adhesion molecule 5
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 32 |
Likely benign | 0 | 12 |
not provided | 1 | 0 |
Uncertain significance | 0 | 66 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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110 |
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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 | CD66e |
SYNONYM | CEA |
MIM | 114890 OMIM |
HGNC | HGNC:1817 HGNC |
Ensembl | ENSG00000105388 Ensembl |
AllianceGenome | HGNC:1817 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000221992.11 | hg38 | chr19 | 41,708,626 | 41,730,433 | 21,808 |
ENST00000398599.8 | hg38 | chr19 | 41,708,585 | 41,729,345 | 20,761 |
ENST00000405816.5 | hg38 | chr19 | 41,708,649 | 41,729,335 | 20,687 |
ENST00000615021.4 | hg38 | chr19 | 41,708,649 | 41,727,352 | 18,704 |
ENST00000617332.4 | hg38 | chr19 | 41,708,649 | 41,727,352 | 18,704 |
ENST00000398599.8 | hg19 | chr19 | 42,212,504 | 42,233,265 | 20,762 |
ENST00000221992.11 | hg19 | chr19 | 42,212,545 | 42,234,353 | 21,809 |
ENST00000615021.4 | hg19 | chr19 | 42,212,568 | 42,231,272 | 18,705 |
ENST00000617332.4 | hg19 | chr19 | 42,212,568 | 42,231,272 | 18,705 |
ENST00000405816.5 | hg19 | chr19 | 42,212,568 | 42,233,255 | 20,688 |
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