PVRIG PVR related immunoglobulin domain containing
Information
- Symbol
- PVRIG
- Type
- protein-coding
- Description
- PVR related immunoglobulin domain containing
- Entrez Gene ID
- 79037
- Genome
- hg19
- Position
- chr7:99,816,243-99,819,113
- Genome
- hg38
- Position
- chr7:100,218,620-100,221,490
- MIM
- 617012 OMIM
- HGNC
- HGNC:32190 HGNC
- Ensembl
- ENSG00000213413 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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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 |
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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 |
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 |
---|---|
SYNONYM | C7orf15 |
SYNONYM | CD112R |
MIM | 617012 OMIM |
HGNC | HGNC:32190 HGNC |
Ensembl | ENSG00000213413 Ensembl |
AllianceGenome | HGNC:32190 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000699088.1 | hg38 | chr7 | 100,219,949 | 100,221,490 | 1,542 |
ENST00000317271.3 | hg38 | chr7 | 100,218,620 | 100,221,490 | 2,871 |
ENST00000317271.3 | hg19 | chr7 | 99,816,243 | 99,819,113 | 2,871 |
ENST00000699088.1 | hg19 | chr7 | 99,817,572 | 99,819,113 | 1,542 |
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