SLC22A18AS SLC22A18 antisense RNA
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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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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 |
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SYNONYM | BWR1B |
SYNONYM | BWSCR1B |
SYNONYM | ORCTL2S |
SYNONYM | SLC22A1LS |
SYNONYM | p27-BWR1B |
MIM | 603240 OMIM |
HGNC | HGNC:10965 HGNC |
Ensembl | ENSG00000254827 Ensembl |
AllianceGenome | HGNC:10965 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000625099.4 | hg38 | chr11 | 2,887,344 | 2,903,575 | 16,232 |
ENST00000625099.4 | hg19 | chr11 | 2,908,574 | 2,924,805 | 16,232 |
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