VSIG10L2 V-set and immunoglobulin domain containing 10 like 2
Information
- Symbol
- VSIG10L2
- Type
- protein-coding
- Description
- V-set and immunoglobulin domain containing 10 like 2
- Entrez Gene ID
- 338667
- Genome
- hg19
- Position
- chr11:125,815,939-125,826,214
- Genome
- hg38
- Position
- chr11:125,946,044-125,956,319
- HGNC
- HGNC:27879 HGNC
- Ensembl
- ENSG00000283703 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 52 |
Likely benign | 0 | 14 |
Uncertain significance | 0 | 94 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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4 |
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154 |
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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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000686984.1 | hg38 | chr11 | 125,946,044 | 125,956,319 | 10,276 |
ENST00000638636.2 | hg38 | chr11 | 125,946,056 | 125,958,647 | 12,592 |
ENST00000686984.1 | hg19 | chr11 | 125,815,939 | 125,826,214 | 10,276 |
ENST00000638636.2 | hg19 | chr11 | 125,815,951 | 125,828,542 | 12,592 |
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