IGFLR1 IGF like family receptor 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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56 |
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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 |
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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 | TMEM149 |
MIM | 614143 OMIM |
HGNC | HGNC:23620 HGNC |
Ensembl | ENSG00000126246 Ensembl |
AllianceGenome | HGNC:23620 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000592889.1 | hg38 | chr19 | 35,739,157 | 35,741,335 | 2,179 |
ENST00000246532.6 | hg38 | chr19 | 35,738,801 | 35,742,452 | 3,652 |
ENST00000588992.5 | hg38 | chr19 | 35,739,215 | 35,742,453 | 3,239 |
ENST00000592537.5 | hg38 | chr19 | 35,739,254 | 35,742,447 | 3,194 |
ENST00000246532.6 | hg19 | chr19 | 36,229,702 | 36,233,353 | 3,652 |
ENST00000592889.1 | hg19 | chr19 | 36,230,058 | 36,232,236 | 2,179 |
ENST00000588992.5 | hg19 | chr19 | 36,230,116 | 36,233,354 | 3,239 |
ENST00000592537.5 | hg19 | chr19 | 36,230,155 | 36,233,348 | 3,194 |
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