CAMKV CaM kinase like vesicle associated
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 20 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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28 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | 1G5 |
| SYNONYM | VACAMKL |
| MIM | 614993 OMIM |
| HGNC | HGNC:28788 HGNC |
| Ensembl | ENSG00000164076 Ensembl |
| AllianceGenome | HGNC:28788 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000463537.5 | hg38 | chr3 | 49,857,989 | 49,869,931 | 11,943 |
| ENST00000466940.5 | hg38 | chr3 | 49,859,293 | 49,869,909 | 10,617 |
| ENST00000488336.5 | hg38 | chr3 | 49,857,989 | 49,869,906 | 11,918 |
| ENST00000296471.11 | hg38 | chr3 | 49,857,989 | 49,869,905 | 11,917 |
| ENST00000467248.5 | hg38 | chr3 | 49,859,261 | 49,869,906 | 10,646 |
| ENST00000477224.6 | hg38 | chr3 | 49,857,989 | 49,869,906 | 11,918 |
| ENST00000620470.4 | hg38 | chr3 | 49,859,255 | 49,862,388 | 3,134 |
| ENST00000296471.11 | hg19 | chr3 | 49,895,422 | 49,907,338 | 11,917 |
| ENST00000466940.5 | hg19 | chr3 | 49,896,726 | 49,907,342 | 10,617 |
| ENST00000463537.5 | hg19 | chr3 | 49,895,422 | 49,907,364 | 11,943 |
| ENST00000467248.5 | hg19 | chr3 | 49,896,694 | 49,907,339 | 10,646 |
| ENST00000488336.5 | hg19 | chr3 | 49,895,422 | 49,907,339 | 11,918 |
| ENST00000477224.6 | hg19 | chr3 | 49,895,422 | 49,907,339 | 11,918 |
| ENST00000620470.4 | hg19 | chr3 | 49,896,688 | 49,899,821 | 3,134 |
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