ELAVL3 ELAV like RNA binding protein 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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 |
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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Category | : |
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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 | HUC |
SYNONYM | HUCL |
SYNONYM | PLE21 |
MIM | 603458 OMIM |
HGNC | HGNC:3314 HGNC |
Ensembl | ENSG00000196361 Ensembl |
AllianceGenome | HGNC:3314 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000438662.6 | hg38 | chr19 | 11,454,403 | 11,480,625 | 26,223 |
ENST00000359227.8 | hg38 | chr19 | 11,451,326 | 11,481,046 | 29,721 |
ENST00000359227.8 | hg19 | chr19 | 11,562,141 | 11,591,861 | 29,721 |
ENST00000438662.6 | hg19 | chr19 | 11,565,218 | 11,591,440 | 26,223 |
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