RERGL RERG like
Information
- Symbol
- RERGL
- Type
- protein-coding
- Description
- RERG like
- Entrez Gene ID
- 79785
- Genome
- hg19
- Position
- chr12:18,233,803-18,243,127
- Genome
- hg38
- Position
- chr12:18,080,869-18,090,193
- HGNC
- HGNC:26213 HGNC
- Ensembl
- ENSG00000111404 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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22 |
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2 |
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 |
Prediction | |||||
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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 |
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ENST00000536890.1 | hg38 | chr12 | 18,081,337 | 18,090,141 | 8,805 |
ENST00000229002.6 | hg38 | chr12 | 18,080,869 | 18,090,193 | 9,325 |
ENST00000538724.6 | hg38 | chr12 | 18,080,869 | 18,090,193 | 9,325 |
ENST00000229002.6 | hg19 | chr12 | 18,233,803 | 18,243,127 | 9,325 |
ENST00000538724.6 | hg19 | chr12 | 18,233,803 | 18,243,127 | 9,325 |
ENST00000536890.1 | hg19 | chr12 | 18,234,271 | 18,243,075 | 8,805 |
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