VNN3P vanin 3, pseudogene
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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.]
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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 | HSA238982 |
SYNONYM | VNN3 |
MIM | 606592 OMIM |
HGNC | HGNC:16431 HGNC |
Ensembl | ENSG00000293493 Ensembl |
AllianceGenome | HGNC:16431 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000519686.6 | hg38 | chr6 | 132,722,926 | 132,734,692 | 11,767 |
ENST00000544102.1 | hg38 | chr6 | 132,726,994 | 132,734,333 | 7,340 |
ENST00000414302.7 | hg38 | chr6 | 132,722,787 | 132,734,756 | 11,970 |
ENST00000425515.7 | hg38 | chr6 | 132,722,787 | 132,734,779 | 11,993 |
ENST00000580813.1 | hg38 | chr6 | 132,728,912 | 132,730,660 | 1,749 |
ENST00000427187.7 | hg38 | chr6 | 132,722,787 | 132,734,772 | 11,986 |
ENST00000423615.7 | hg38 | chr6 | 132,722,784 | 132,734,772 | 11,989 |
ENST00000367927.10 | hg38 | chr6 | 132,722,787 | 132,734,767 | 11,981 |
ENST00000392393.7 | hg38 | chr6 | 132,722,926 | 132,734,765 | 11,840 |
ENST00000275223.8 | hg38 | chr6 | 132,722,787 | 132,734,692 | 11,906 |
ENST00000450865.2 | hg38 | chr6 | 132,724,921 | 132,734,765 | 9,845 |
ENST00000423615.7 | hg19 | chr6 | 133,043,923 | 133,055,911 | 11,989 |
ENST00000275223.8 | hg19 | chr6 | 133,043,926 | 133,055,831 | 11,906 |
ENST00000414302.7 | hg19 | chr6 | 133,043,926 | 133,055,895 | 11,970 |
ENST00000367927.10 | hg19 | chr6 | 133,043,926 | 133,055,906 | 11,981 |
ENST00000427187.7 | hg19 | chr6 | 133,043,926 | 133,055,911 | 11,986 |
ENST00000425515.7 | hg19 | chr6 | 133,043,926 | 133,055,918 | 11,993 |
ENST00000519686.6 | hg19 | chr6 | 133,044,065 | 133,055,831 | 11,767 |
ENST00000392393.7 | hg19 | chr6 | 133,044,065 | 133,055,904 | 11,840 |
ENST00000450865.2 | hg19 | chr6 | 133,046,060 | 133,055,904 | 9,845 |
ENST00000544102.1 | hg19 | chr6 | 133,048,133 | 133,055,472 | 7,340 |
ENST00000580813.1 | hg19 | chr6 | 133,050,051 | 133,051,799 | 1,749 |
Key | Value |
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strand | - |
start | 133,043,925 |
Gene Symbol | VNN3 |
Entrez GeneId | 55,350 |
Chr Band | 6q23.2 |
end | 133,055,903 |
chr | chr6 |
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