PLAC8 placenta associated 8
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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8 |
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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
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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 |
Prediction | |||||
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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 | |||
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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 | C15 |
SYNONYM | DGIC |
SYNONYM | PNAS-144 |
SYNONYM | onzin |
MIM | 607515 OMIM |
HGNC | HGNC:19254 HGNC |
Ensembl | ENSG00000145287 Ensembl |
AllianceGenome | HGNC:19254 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000411416.6 | hg38 | chr4 | 83,090,688 | 83,109,843 | 19,156 |
ENST00000311507.9 | hg38 | chr4 | 83,090,048 | 83,114,729 | 24,682 |
ENST00000505406.5 | hg38 | chr4 | 83,090,806 | 83,137,075 | 46,270 |
ENST00000426923.2 | hg38 | chr4 | 83,092,861 | 83,114,715 | 21,855 |
ENST00000509973.5 | hg38 | chr4 | 83,090,793 | 83,114,736 | 23,944 |
ENST00000311507.9 | hg19 | chr4 | 84,011,201 | 84,035,882 | 24,682 |
ENST00000411416.6 | hg19 | chr4 | 84,011,841 | 84,030,996 | 19,156 |
ENST00000509973.5 | hg19 | chr4 | 84,011,946 | 84,035,889 | 23,944 |
ENST00000505406.5 | hg19 | chr4 | 84,011,959 | 84,058,228 | 46,270 |
ENST00000426923.2 | hg19 | chr4 | 84,014,014 | 84,035,868 | 21,855 |
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