TRPV2 transient receptor potential cation channel subfamily V member 2
Information
- Symbol
- TRPV2
- Type
- protein-coding
- Description
- transient receptor potential cation channel subfamily V member 2
- Entrez Gene ID
- 51393
- Genome
- hg19
- Position
- chr17:16,318,885-16,340,317
- Genome
- hg38
- Position
- chr17:16,415,571-16,437,003
- MIM
- 606676 OMIM
- HGNC
- HGNC:18082 HGNC
- Ensembl
- ENSG00000187688 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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68 |
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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
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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 |
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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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | VRL |
SYNONYM | VRL-1 |
SYNONYM | VRL1 |
MIM | 606676 OMIM |
HGNC | HGNC:18082 HGNC |
Ensembl | ENSG00000187688 Ensembl |
AllianceGenome | HGNC:18082 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000338560.12 | hg38 | chr17 | 16,415,571 | 16,437,003 | 21,433 |
ENST00000338560.12 | hg19 | chr17 | 16,318,885 | 16,340,317 | 21,433 |
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