LOH12CR2 loss of heterozygosity on chromosome 12, region 2
Information
- Symbol
- LOH12CR2
- Type
- ncRNA
- Description
- loss of heterozygosity on chromosome 12, region 2
- Entrez Gene ID
- 503693
- Genome
- hg19
- Position
- chr12:12,508,337-12,510,001
- Genome
- hg38
- Position
- chr12:12,355,403-12,357,067
- HGNC
- HGNC:26524 HGNC
- Ensembl
- ENSG00000205791 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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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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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Filtering | : |
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 | LOH2CR12 |
HGNC | HGNC:26524 HGNC |
Ensembl | ENSG00000205791 Ensembl |
AllianceGenome | HGNC:26524 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000381800.4 | hg38 | chr12 | 12,355,403 | 12,357,067 | 1,665 |
ENST00000381800.4 | hg19 | chr12 | 12,508,337 | 12,510,001 | 1,665 |
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