PVR PVR cell adhesion molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 6 | 14 |
Likely benign | 0 | 14 |
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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80 |
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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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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 | CD155 |
SYNONYM | HVED |
SYNONYM | NECL5 |
SYNONYM | Necl-5 |
SYNONYM | PVS |
SYNONYM | TAGE4 |
MIM | 173850 OMIM |
HGNC | HGNC:9705 HGNC |
Ensembl | ENSG00000073008 Ensembl |
AllianceGenome | HGNC:9705 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000406449.8 | hg38 | chr19 | 44,644,097 | 44,659,094 | 14,998 |
ENST00000403059.8 | hg38 | chr19 | 44,643,910 | 44,663,583 | 19,674 |
ENST00000344956.8 | hg38 | chr19 | 44,643,798 | 44,663,583 | 19,786 |
ENST00000706606.1 | hg38 | chr19 | 44,643,872 | 44,655,567 | 11,696 |
ENST00000706603.1 | hg38 | chr19 | 44,643,820 | 44,663,562 | 19,743 |
ENST00000425690.8 | hg38 | chr19 | 44,643,910 | 44,666,162 | 22,253 |
ENST00000344956.8 | hg19 | chr19 | 45,147,098 | 45,166,850 | 19,753 |
ENST00000706603.1 | hg19 | chr19 | 45,147,120 | 45,166,829 | 19,710 |
ENST00000706606.1 | hg19 | chr19 | 45,147,172 | 45,158,834 | 11,663 |
ENST00000403059.8 | hg19 | chr19 | 45,147,210 | 45,166,850 | 19,641 |
ENST00000425690.8 | hg19 | chr19 | 45,147,210 | 45,169,430 | 22,221 |
ENST00000406449.8 | hg19 | chr19 | 45,147,397 | 45,162,362 | 14,966 |
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